customer advisory vs. Ayala Center Makati
Office of Makati City Administrator accepted
complaint vs. Ayala Center Makati
Evidence that the Office of the City Administrator of Makati accepted my complaint vs. Ayala Center Makati is a letter identified as originating from a source identified as Marjorie A. De Veyra Acting City administrator and dated October 6, 2009.
Prior to what was described as a robbery incident at Rolex store at Greenbelt 5, Ayala Center, Makati, security lapses repeatedly occurred at entrances to different shopping areas at said center. Because of said security lapses I could repeatedly have brought deadly weapons into said areas, to the detriment of customers inside said areas.At the Glorietta, Ayala mall, Ayala Center, Makati, there was a defect in the enclosure for the handicapped.After I entered said enclosure, I had difficulty . in getting out of said enclosure. I had to kick several times the door of said enclosure before I was able to exit. The person in charge of said enclosure was identified as Francisco Diola.On August 4, 2009, a person, identified as Madel Enriquez, allegedly from the Concierge at said Glorietta, received my complaint regarding said defective enclosure. Said complaint was addressed to Patrick Avila of Glorietta. Up to October 30, 2009 no one from Ayala Malls Group has provided me with an apology for said incident. I have evidence that persons, identified as Myrna Cruz-Fernandez Assistant Vice President Ayala Malls Group, Mina C. Domingo Operations Officer Ayala Malls Group, Patrick John C. Avila Operations Officer Ayala Malls Group were aware of said defective door,

I have seen Belkin brand products being sold locally.
Belkin International Inc. Recalls SurgeMaster™ Surge Protectors Due to Shock Hazard
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10024.html
NEWS from CPSC
U.S. Consumer Product Safety Commission
Office of Information and Public Affairs Washington, DC 20207

FOR IMMEDIATE RELEASE
October 27, 2009
Release # 10-024 Firm's Recall Hotline: (800) 952-1465
CPSC Recall Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
Belkin International Inc. Recalls SurgeMaster™ Surge Protectors Due to Shock Hazard

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: SurgeMaster™ Surge Protectors

Units: About 68,700

Importer: Belkin International Inc., of Compton, Calif.

Hazard: The molding of the plastic 360 degree rotating plug, which allows for easy cord movement, can crack or detach from the plug assembly, posing a shock hazard to consumers.

Incidents/Injuries: Belkin has received seven consumer complaints about cracking of the plug molding. No injuries were reported.

Description: This recall involves the SurgeMaster™ Surge Protector, models F9G930-10, F9G930v10, F9G930-10-W and F9G930-10-SN, all manufactured in 2003. The model number and date of manufacture are located on the underside of the unit. Grey models F9G930-10-GRY and F9G930fc10G-CL are not a part of this recall.

Sold by: Independent distributors nationwide and the internet by www.belkin.com from September 2003 through December 2007 for about $50.

Manufactured in: China

Remedy: Consumers should stop using these power strips immediately and contact Belkin for a new replacement unit.
__________________________________________________________________________________________________________________________________________________
I have seen Coby products sold locally.
Coby Electronics Recalls Rechargeable Batteries Sold with Portable DVD_CD_MP3 Players Due to Fire Hazard
NEWS from CPSC
U.S. Consumer Product Safety Commission
Office of Information and Public Affairs Washington, DC 20207

FOR IMMEDIATE RELEASE
October 22, 2009
Release # 10-019 Firm's Recall Hotline: (877) 305-2629
CPSC Recall Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
Coby Electronics Recalls Rechargeable Batteries Sold with Portable DVD/CD/MP3 Players Due to Fire Hazard

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Rechargeable batteries sold with portable DVD/CD/MP3 players

Units: About 19,600

Importer: Coby Electronics Corp., of Lake Success N.Y.

Hazard: The rechargeable batteries can overheat, posing a fire hazard to consumers.

Incidents/Injuries: Coby Electronics has received 10 reports of batteries overheating, including eight reports of fires resulting in property damage. No injuries have been reported.

Description: The recall involves Coby DVD/CD/MP3 players with an 8 ½ inch screen and product number TF-DVD- 8501. The rechargeable batteries sold with the DVD players have serial numbers that begin with “HY.” The serial number can be found on a white sticker affixed to the battery. “Coby” is printed on the front cover and the product number is on the bottom of the unit.

Sold at: Discount, electronics, music, toy, office supply stores and distributors of electronic products nationwide from January 2007 through September 2009 for between $140 and $275.

Manufactured in: China

Remedy: Consumers should immediately remove the recalled batteries from the unit and contact Coby Electronics to receive a free replacement battery. Consumers can continue to use the DVD/CD/MP3 players with AC or DC power adapters.

Consumer Contact: For additional information, contact Coby Electronics toll-free at (877) 305-2629 between 8 a.m. and 5 p.m. ET Monday through Friday, or visit the firm’s Web site at www.cobyusa.com
_______________________________________________________________________________________________________________________________________________________________________________________________________
FDA New Online Guide to Hearing Aids
http://www.fda.gov/ForConsumers/ConsumerUpdates/ucm185723.htm
_______________________________________________________________________________________________________________________________________________________________________________________________________
Sony Recalls Computer AC Adapters Due to Shock Hazard
http://www.cpsc.gov/cpscpub/prerel/prhtml10/10027.html
NEWS from CPSC
U.S. Consumer Product Safety Commission
Office of Information and Public Affairs Washington, DC 20207

FOR IMMEDIATE RELEASE
October 28, 2009
Release # 10-027 Firm's Recall Hotline: (877) 361-4481
CPSC Recall Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
Firm’s Media Contact: (858) 942-2905
Sony Recalls Computer AC Adapters Due to Shock Hazard

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Sony VAIO Computer AC Adapters

Units: About 69,000

Manufacturer: Sony Electronics Inc. of San Diego, Calif.

Hazard: Insulation inside the AC adapter can fail over time, posing an electrical shock hazard to consumers.

Incidents/Injuries: Sony has received four reports of adapters short circuiting. No incidents occurred in the United States. No injuries have been reported.

Description: The recalled AC adapter model is the Sony VGP-AC19V17, which was supplied for use with the following Sony products:
Product Types Using the AC Adapters Product Models Using the AC Adapters
All-in-one VAIO Desktop Computers VGC-LT series and VGC-JS2 series
VAIO Docking Stations VGP-PRBX1 and VGP-PRFE1

Sold at: The SonyStyle stores and Web site, authorized electronics retailers and authorized business- to- business dealers nationwide from September 2005 through October 2009 for between $900 and $3300 for desktop computers and $250 and $300 for docking stations.

Manufactured in: China

Remedy: Consumers should turn off their computer, unplug it and stop using the recalled AC adapters immediately and contact Sony to arrange for a free replacement of the affected AC adapter.

Consumer Contact: For more information, contact Sony toll-free at (877) 361-4481 anytime, or visit the firm’s Web site at esupport.sony.com/ac19adapter
________________________________________________________________________________________________________________________________________________________________________________________________
The National Library of Medicine's Household Products Database.
http://hpd.nlm.nih.gov/
What's under your kitchen sink, in your garage, in your bathroom, and on the shelves in your laundry room?
Learn more about what's in these products, about potential health effects, and about safety and handling.

Browse by category:
Auto Products
Inside the Home
Pesticides
Landscape/Yard
Personal Care
Home Maintenance
Arts & Crafts
Pet Care
Home Office

Browse A to Z:
Product Names
Types of Products
Manufacturers
Ingredients
Support pages
About the Database
FAQ
Product Recalls
Help
Glossary
___________________________________________________________________________________________________________________________________________________________
Unilever Issues Allergy Alert on Wheat in a Limited Number of Tubs of Breyers® Ice Cream (Fri, 23 Oct 2009 14:11:00 -0400) Unilever United States, Inc., of Englewood Cliffs, NJ, in cooperation with the U.S. Food and Drug Administration (FDA), is voluntarily recalling a limited number of tubs of Breyers® ice cream because it was mispackaged and may contain undeclared wheat. People who have an allergy or severe sensitivity to wheat run the risk of allergic reaction if they consume this product...
http://www.recalls.gov/recent.html

Customer advisory vs. National Book store branch at Robinsons Ermita. Because of lax security at street entrance to said store, I could have, on October 27, 2009,
have brought deadly weapons into said store and into different areas of Robinsons
Ermita.


Customer advisory vs. SM mall at San Lazaro, Manila. Because of lax security at entrance to said mall, on October 27, 2009, I could have brought deadly weapons
into said mall,including SM Supermarket The employee at the package counter
of said store allowed me to deposit said luggage at said area without
first inspecting the contents of said luggage. Said luggage was large enough to contain deadly weapons.


Warning vs. employees at Jollibee store at SM San Lazaro, Manila.Said employees were identified as "Effren" and "Rosette" On October 27, 2009, I saw said Effren
sweeping the floor at the dining area of said store while customers were eating
at said store. So the dust stirred up by said sweeping could land on the food
the customers were eating. Said Rosalyn gave me a hot dog sandwich with cheese when I ordered a hot dog sandwich with only a hot dog and bread. The person who received my payment and my order was identified as Rosette
and the official receipt issued was identified as #377539..

Lax security on October 21, 2009 at entrances to the following areas at Ayala Center, Makati City.

From U.S. FDA web site re General Mills Cheerio claims
http://google2.fda.gov/search?q=Cheerio+claims&x=20&y=20&client=FDAgov&site=FDAgov&lr=&proxystylesheet=FDAgov&output=xml_no_dtd&getfields=*
[PDF] General Mills, Minneapolis, Minnesota. Warning Letter response. 05 ...
... The statements on the Cheerios® label about lowering ... is disallowed under the health
claim regulation at ... regulation, FDA explained that the claims should "not ...
www.fda.gov/downloads/AboutFDA/CentersOffices/ORA/ORAElectronicReadingRoom/UCM167463.pdf - Text Version
___________________________________________________________________________________________________
Childhood Lead Poisoning Prevention
http://www.cdc.gov/Features/LeadPoisoning/
Lead poisoning is entirely preventable. The key is stopping children from coming into contact with lead and treating children who have been poisoned by lead. Learn more about preventing childhood lead poisoning and National Lead Poisoning Prevention Week activities.


Childhood Lead Exposure


Young children often place their toys, fingers, and other objects in their mouth as part of their normal development, this hand-to-mouth activity may put them in contact with lead paint or dust.

The most common sources of lead exposure for children are chips and particles of old lead paint. Although children may be directly exposed to lead from paint by swallowing paint chips, they are more commonly exposed by swallowing house dust or soil contaminated by leaded paint. This happens because lead paint chips become ground into tiny bits that become part of the dust and soil in and around homes. This usually occurs when leaded paint becomes old or worn or is subject to constant rubbing (as on doors and windowsills and wells). In addition, lead can be scattered when paint is disturbed during destruction, remodeling, paint removal, or preparation of painted surfaces for repainting.

Lead, which is invisible to the naked eye and has no smell, may be found in other sources. These sources may be the exposure source for as many as 30% of lead-poisoned children in certain areas across the United States. They include

* traditional home health remedies such as azarcon and greta, which are used for upset stomach or indigestion in the Hispanic community
* imported candies
* imported toys and toy jewelry
* imported cosmetics
* pottery and ceramics
* drinking water contaminated by lead leaching from lead pipes, solder, brass fixtures, or valves and
* consumer products, including tea kettles and vinyl miniblinds

Additionally, a variety of work and hobby activities and products expose adults to lead. This also can result in lead exposure for their families. Activities that are associated with lead exposure include indoor firing range use, home repairs and remodeling, and pottery making. "Take-home" exposures may result when people whose jobs expose them to lead wear their work clothes home or wash them with the family laundry. It also may result when they bring scrap or waste material home from work.
Protecting Children from Lead Exposure

Lead poisoning is entirely preventable. The key is stopping children from coming into contact with lead and treating children who have been poisoned by lead.

The goal is to prevent lead exposure to children before they are harmed. There are many ways parents can reduce a child's exposure to lead. The key is stopping children from coming into contact with lead. Lead hazards in a child's environment must be identified and controlled or removed safely.
Concern about Your Child's Exposure

If you have any reason to suspect that your child has been exposed to lead contact your health care provider. Your child's health care provider can help you decide whether to perform a blood test to see if your child has an elevated blood lead level. A blood lead test is the only way you can tell if your child has an elevated lead level. Most children with elevated blood lead levels have no symptoms. The health care provider can recommend treatment if your child has been exposed to lead.

See frequently asked questions about lead and possible lead exposure.

For more information on sources of lead exposure and prevention tips, please visit our Web site at www.cdc.gov/nceh/lead or call the CDC-INFO at 1-800-CDC-INFO (232-4636).
___________________________________________________________________________________________________________________________________________________________________________
FDA MedWatch - September 2009 Drug Safety Labeling Changes - 36 drugs with changes to Boxed Warning, Warnings, Contraindications, Precautions, Adverse Reactions
Tuesday, October 20, 2009 3:18 AM

The MedWatch September 2009 Drug Safety Labeling Changes posting includes 36 drug products with safety labeling changes to the following sections: BOXED WARNING, CONTRAINDICATIONS, WARNINGS, PRECAUTIONS, ADVERSE REACTIONS, PATIENT PACKAGE INSERT, and MEDICATION GUIDE.

The "Summary Page" provides a listing of drug names and safety labeling sections revised: http://www.fda.gov/Safety/MedWatch/SafetyInformation/ucm183107.htm

Clicking on a drug product name in the Summary View will take you to the "detailed view" page, which identifies safety labeling sections and subsections revised, along with a brief summary of new or modified safety information to the BOXED WARNING, CONTRAINDICATIONS, and/or WARNINGS sections.

The following drugs had modifications to the BOXED WARNING, CONTRAINDICATIONS, and WARNINGS sections:

AndroGel (testosterone gel), Rapamune (sirolimus), Testim (testosterone gel), Cordarone (amiodarone HCl), Flector Patch (diclofenac epolamine), Intelence (etravirine), Kayexalate (sodium polystyrene sulfonate), Lexiva (fosamprenavir calcium), Neoral (cyclosporine capsules, modified), Ortho Evra (norelgestromin/ethinyl estradiol) transdermal system, Pre-Pen (benzylpenicilloyl polylysine), Sustiva (efavirenz), Ultracet (tramadol HCl/acetaminophen), Ultram (tramadol hydrochloride), Voltaren Gel (diclofenac sodium), Zolinza (vorinostat).

_____________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________
web site that may contain useful information:

life123 com web site
http://www.life123.com/

_____________________________________________________________________________________________________________________________________________________________
New edition of NIH Research Matters at a new location
http://us.mc343.mail.yahoo.com/mc/welcome?.gx=1&.tm=1256019166&.rand=3n24nrt4ddbsj#_pg=showMessage&sMid=7&&filterBy=&.rand=1635259440&midIndex=7&mid=1_22282720_AIiyo0IAARvGStzN5AvN8yUqmTA&m=1_22288679_AIqyo0IAAIXXStz09QjIaicG0qw,1_22286093_AIeyo0IAAF8yStztKw6xLS7UKU8,1_22280225_AIqyo0IAAGEfStzE9AIJfHZFNXw,1_22278658_AIayo0IAAWryStzEeAqilXxX6us,1_22277879_AImyo0IAAD7hStzBaAyTkFJvj%2Fw,1_22282720_AIiyo0IAARvGStzN5AvN8yUqmTA,1_22277188_AIuyo0IAAVarStzBQAuGunpokvk,1_22275941_AIeyo0IAAFIiSty%2FiwqCAX304PQ,1_22275205_AIqyo0IAAD%2BCSty%2FSwkVOX5EmBI,1_22274668_AIqyo0IAADJFSty%2BTgRsUj9xVrY,1_22283399_AIqyo0IAAQtLStzXQgba53PHhI0,&sort=date&order=down&startMid=0&pSize=25&hash=cb6417217c6cc7d8d9d8ef9c95261d6b&.jsrand=9083649

_____________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________

Recently, I passed by the compound of St. Paul's university at P. Gil St., Ermita,
Manila. I saw a dirty worn Philippine national flag on display within said compound.
That indicates disrespect for said flag.
___________________________________________________________________________________


U.S. Coast Guard's Boating Safety Division
http://www.uscgboating.org/

The U.S. Coast Guard's Boating Safety Division (CG-5422) is dedicated to reducing loss of life, injuries, and property damage that occur on U.S. waterways by improving the knowledge, skills, and abilities of recreational boaters.
Strategic Plan

Read about the Strategic Plan of the National Recreational Boating Safety Program.
Vision/Mission




USCG Boating Safety Division Facts, FAQs, and Org Chart

A list of frequently asked questions on a variety of safe boating topics. Discover what the Coast Guard does on an average day.
Partnerships



Learn and network with others interested in boating safety.

RESOURCES
Media and Marketing Materials

Members of the press, boating safety specialists and advocates, and the general public are invited to utilize any and all of the media and marketing materials in this section.

Photo Library

The U.S. Coast Guard has provided the Image Library as a resource tool for boating safety specialists, advocates and the general public.

Video Library

The U.S. Coast Guard has provided the Video Library as a resource tool for boating safety specialists, advocates and the general public.






LIFE JACKET WEAR / WEARING YOUR LIFE JACKET

Boaters enjoy the feel of sun and spray. So it’s tempting to boat without wearing a life jacket – especially on nice days. But modern life jackets are available in a wide variety of shapes, colors, and sizes. Many are thin and flexible. Some are built right into fishing vests or hunter coats. Others are inflatable — as compact as a scarf or fanny pack until they hit water, when they automatically fill with air.

There’s no excuse not to wear a life jacket on the water!

How to Choose the Right Life Jacket Brochure - PDF

Things to Know:

* Certain life jackets are designed to keep your head above water and help you remain in a position which permits proper breathing.

* To meet U.S. Coast Guard requirements, a boat must have a U.S. Coast Guard-approved Type I, II, III, or V life jacket for each person aboard. Boats 16 feet and over must have at least one Type IV throwable device as well.

* All states have regulations regarding life jacket wear by children.

* Adult-sized life jackets will not work for children. Special life jackets are available. To work correctly, a life jacket must be worn, fit snugly, and not allow the child’s chin or ears to slip through.

* Life jackets should be tested for wear and buoyancy at least once each year. Waterlogged, faded, or leaky jackets should be discarded.

* Life jackets must be properly stowed.

* A life jacket — especially a snug-fitting flotation coat or deck-suit style — can help you survive in cold water.

How Do Life Jackets Save Lives?

* When capsized in rough water.
* When sinking in unexpectedly heavy sea conditions.
* When thrown from the boat as a result of a collision.
* When injured by rocks or submerged objects.
* When unconscious from carbon monoxide fumes.
* When tossed into freezing water.
* When thrown off balance while fishing.
* When unable to swim because of heavy or waterlogged clothing.


All recreational boats must carry one wearable lifejacket (Type I, II, III or Type V lifejacket) for each person aboard. A Type V lifejacket provides performance of either a Type I, II, or III lifejacket (as marked on its label) and must be used according to the label requirements. Any boat 16ft and longer (except canoes and kayaks) must also carry one throwable lifejacket (Type IV lifejacket).

Lifejackets must be

* Coast Guard approved,
* in good and serviceable condition, and
* the appropriate size for the intended user.

Accessibility

* Wearable lifejackets must be readily accessible.
* You must be able to put them on in a reasonable amount of time in an emergency (vessel sinking, on fire, etc.).
* They should not be stowed in plastic bags, in locked or closed compartments or have other gear stowed on top of them.
* The best lifejacket is the one you will wear.
* Though not required, a lifejacket should be worn at all times when the vessel is underway. A wearable lifejacket can save your life, but only if you wear it.
* Throwable devices must be immediately available for use.

Inflatable Lifejackets

* Inflatable lifejackets may be more comfortable to wear.
* The best lifejacket is the one you will wear.
* Inflatable lifejackets require the user to pay careful attention to the condition of the device.
* Inflatable lifejackets must have a full cylinder and all status indicators on the inflator must be green, or the device is NOT serviceable, and does NOT satisfy the requirement to carry lifejackets.
* Coast Guard Approved Inflatable lifejacket's are authorized for use on recreational boats by person at least 16 years of age.

Child Lifejacket Requirements

Some states require that children wear lifejackets

* applies to children of specific ages
* applies to certain sizes of boats
* applies to specific boating operations

Check with your state boating safety officials.

Child lifejacket approvals are based on the child's weight. Check the "User Weight" on the label, or the approval statement that will read something like "Approved for use on recreational boats and uninspected commercial vessels not carrying passengers for hire, by persons weighing __ lbs". They can be marked "less than 30", "30 to 50", "less than 50", or "50 to 90".

Lifejacket requirements for certain boating activities under state laws

The Coast Guard recommends and many states require wearing lifejackets:

* For water skiing and other towed activities (use a lifejacket marked for water skiing).
* While operating personal watercraft (PWC) (use a lifejacket marked for water skiing or PWC use).
* During white water boating activities.
* While sailboarding (under Federal law, sailboards are not "boats").

Check with your state boating safety officials.

Federal law does not require lifejackets on racing shells, rowing sculls, racing canoes, and racing kayaks; state laws vary. Check with your state boating safety officials.

If you are boating in an area under the jurisdiction of the Army Corps of Engineers, or a federal, state, or local park authority, other rules may apply.

Lifejacket Flotation

There are three basic kinds of lifejacket flotation in the five types of lifejackets with the following characteristics:

Inherently Buoyant (primarily Foam)

* Adult, Youth, Child, and Infant sizes
* For swimmers & non-swimmers
* Wearable & throwable styles
* Some designed for water sports


Minimum Buoyancy
Wearable Size Type Inherent Buoyancy (Foam)
Adult I
II & III
V 22 lb.
15.5 lb.
15.5 to 22 lb.
Youth II & III
V 11 lb.
11 to 15.5 lb.
Child and Infant II 7 lb.
Throwable:
Cushion
Ring Buoy IV 20 lb.
16.5 & 32 lb.


Inflatable

* The most compact
* Sizes only for adults
* Only recommended for swimmers
* Wearable styles only
* Some with the best in-water performance


Minimum Buoyancy
Wearable Size Type Inherent Buoyancy
Adult I & II
III
V 34 lb.
22.5 lb.
22.5 to 34 lb.


Hybrid (Foam & Inflation)

* Reliable
* Adult, Youth, and Child sizes
* For swimmers & non-swimmers
* Wearable styles only
* Some designed for water sports

Minimum Buoyancy
Wearable Size Type Inherent Buoyancy Inflated Total Buoyancy
Adult II & III
V 10 lb
7.5 lb. 22 lb.
22 lb.
Youth II & III
V 9 lb
7.5 lb. 15 lb.
15 lb.
Child II 7 lb. 12 lb.

RESOURCES
Media and Marketing Materials

Members of the press, boating safety specialists and advocates, and the general public are invited to utilize any and all of the media and marketing materials in this section.

Photo Library

The U.S. Coast Guard has provided the Image Library as a resource tool for boating safety specialists, advocates and the general public.

Video Library

The U.S. Coast Guard has provided the Video Library as a resource tool for boating safety specialists, advocates and the general public.






ABOUT US

The U.S. Coast Guard's Boating Safety Division (CG-5422) is dedicated to reducing loss of life, injuries, and property damage that occur on U.S. waterways by improving the knowledge, skills, and abilities of recreational boaters.
CONTACT US

For question, concerns and suggestions, please feel free to send us a message. We look forward to your feedback.
Contact Form

Commandant (CG-5422)
U.S. Coast Guard Headquarters
2100 Second St. SW Stop 7581
Washington, DC 20593-7581


U.S. Coast Guard
WWW.USCGBOATING.ORG

* Customer Accessibility
* Webmaster (Technical Website Issues)
* Disclaimer, Privacy & Internet Link Policies
* USCG Home

Last Modified Wednesday April 29, 2009
________________________________________________________________________________________________
phoneticise com web site
http://www.phoneticise.com/

This is an online utility that will phoneticise any text that you enter in the above box
What does that mean?

It means that you get a list of letters in the NATO phonetic alphabet (also known as the international radiotelephony spelling alphabet), and names of any other symbols/characters that aren't in that.
What can I use it for?

It is useful for spelling out words and phrases to people to prevent mis-spelling, especially over the phone.
Programming

There should be a programming library (in .NET) and possibly a web service (SOAP) available for you to use soon so you can integrate this into your own programs/websites
Take a look at my programming blog if you are interested in that kind of thing.
_____________________________________________________________________________________________________________________________________________________________________________________________________________
http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm186598.htm
-
FDA NEWS RELEASE

For Immediate Release: Oct. 14, 2009

Media Inquiries: Christopher Kelly, 301-796-4676, christopher.kelly@fda.hhs.gov
Consumer Inquiries: 888-INFO-FDA
New FDA Web Page Lists Disposal Instructions for Select Medicines

The U.S. Food and Drug Administration today launched a Web page for consumers with information on how to dispose of certain drugs, including several high-potency opioids and other selected controlled substances. These medicines have the potential to be harmful, even deadly, in a single dose if taken by someone other than the intended person.

The FDA recommends that these medicines be disposed of by flushing down the sink or toilet. The goal is to keep them away from children and others who could be harmed by taking them accidentally.

Medicines not listed should be thrown away in the household trash after mixing them with some unpalatable substance, such as coffee grounds, and sealing them in a bag or other container. Another option is to dispose of them through drug take back programs, if federal and state law permit.

“The safe disposal of medicines from the home after they are no longer needed is an important concern for the FDA,” said Douglas Throckmorton, M.D., deputy center director of FDA’s Center for Drug Evaluation and Research.

All medicines listed have disposal instructions in their professional prescribing information; however, this information is targeted to health care professionals. The Web page provides clear instructions for consumers on whether a medicine should be flushed or disposed of in the trash.

Throckmorton also said, “The FDA is working with other groups to improve the use of several drug disposal methods, including drug take back programs. However, for some potent medicines that can cause harm or death if inadvertently taken by family members, the FDA currently recommends flushing them down the sink or toilet to immediately and permanently remove them from the home. Simple precautions like these can reduce the likelihood of accidental and potentially dangerous exposure to unused medicines.”

The FDA worked with the White House Office of National Drug Control Policy (ONDCP) to develop the first consumer guidance for proper disposal of prescription drugs. The ONDCP federal guidelines were first issued in February 2007. The 2009 version of the federal guidelines is available at http://www.whitehousedrugpolicy.gov/publications/pdf/prescrip_disposal.pdf.

For more information:

Disposal by Flushing of Certain Unused Medicines: What You Should Know

Medicines Recommended for Disposal by Flushing

#

RSS Feed for FDA News Releases [what is RSS?]

-
-

Page Last Updated: 10/15/2009

__________________________________________________________________________________________________________________________________________________________

Security lapse at on October 15, 2009 at entrance to Harrison Plaza shopping center in Malate, Manila. Because of said security lapse, I could have brought
deadly weapons into said area, to the detriment of shoppers.

On October 15, 2009, ShopWise store at Harrison Plaza sold an imported food product which did not bear a visible (to unaided eye) name and address of the
importer of said product. I believe said store violated the Consumer Act of the Philippines.
__________________________________________________________________________________________________________________________________________________________

Meditation and Health
http://www.cdc.gov/Features/Meditation/

Tell your health care providers about any complementary and alternative practices you use. Give them a full picture of what you do to manage your health. Do not use meditation as a replacement for conventional care or as a reason to postpone seeing a doctor about a medical problem.

Many people practice meditation for a number of health-related purposes. A 2007 national government survey found that 9.4% of respondents had used meditation in the past 12 months.
Photo: People meditating.What is meditation?

The term meditation refers to a group of techniques which may be practiced for many reasons, such as to increase calmness and physical relaxation, to improve psychological balance, to cope with illness, or to enhance overall wellness. Most types of meditation have four elements in common:

A quiet location. Meditation is usually practiced in a quiet place with as few distractions as possible. This can be particularly helpful for beginners.

A specific, comfortable posture. Depending on the type being practiced, meditation can be done while sitting, lying down, standing, walking, or in other positions.

A focus of attention. Focusing one's attention is usually a part of meditation. For example, the meditator may focus on a mantra (a specially chosen word or set of words), an object, or the sensations of the breath.

An open attitude. Having an open attitude during meditation means letting distractions come and go naturally without judging them.
How can meditation affect my health?

It is not fully known what changes occur in the body during meditation; whether they influence health; and, if so, how. Research is under way to find out more about meditation's effects, how it works, and diseases and conditions for which it may be most helpful.

The National Center for Complementary and Alternative Medicine (NCCAM) is the federal government's lead agency for scientific research on complementary and alternative medicine (CAM). It is 1 of the 27 institutes and centers that make up the National Institutes of Health within the U.S. Department of Health and Human Services. Some recent NCCAM-supported studies have been investigating meditation for relieving stress in caregivers for elderly patients with dementia and for relieving asthma symptoms. A study published in the April 2009 issue of Preventing Chronic Disease researched use of meditation and other complementary and alternative practices in patients suffering from arthritis. See full article.
Is meditation right for me?

Meditation is considered to be safe for healthy people but if you are thinking about using meditation practices to prevent asthma attacks, to control high blood pressure, to reduce arthritis pain, or for any other medical reason, be smart.

* Do not use meditation as a replacement for conventional care or as a reason to postpone seeing a doctor about a medical problem.
* Look for published research studies on meditation for the health condition in which you are interested.
* Tell your health care providers about any complementary and alternative practices you use. Give them a full picture of what you do to manage your health. This will help ensure coordinated and safe care.
_______________________________________________________________________________________________________________________________________________________________________________________________________________
Recent Consumer Updates
http://www.fda.gov/ForConsumers/ConsumerUpdates/default.htm
* Reducing Radiation from Medical X-rays (video)
* Cooperative Program Ensures Safe Shellfish (slideshow)
* Cooperative Programs Help Keep Food Safe
* Cooperative Program Ensures Safe Shellfish
* FDA's MedWatch Safety Alerts: September 2009
* Avoiding Medication Mistakes (video)
* Fortify Your Knowledge About Vitamins (video)


FDA NEWS RELEASE

For Immediate Release: Oct. 13, 2009

Media Inquiries: Chris Kelly, 301-796-4676, christopher.kelly@fda.hhs.gov
Consumer Inquiries: 888-INFO-FDA
FDA Acts to Halt Marketing of Unapproved Codeine Sulfate Tablets
Four Companies Required to Stop Making and Distributing Illegal Opioid Pain Relievers
http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm186418.htm

The U.S. Food and Drug Administration today warned four companies that they must stop marketing unapproved codeine sulfate tablets. These drugs are opioid analgesics, commonly called narcotics, that are widely used to treat pain.

These particular products have not received FDA approval and the agency has no evidence that they are safe and effective. Another manufacturer, Roxane Laboratories, markets FDA-approved codeine sulfate tablets and is able to meet the demand for the drug. The FDA does not anticipate a supply problem for codeine sulfate tablets.

“Consumers deserve and expect that their drugs meet modern FDA standards for safety, effectiveness, labeling, and quality. Removing unapproved products that do not meet those standards is an FDA priority,” said Janet Woodcock, M.D., director of the FDA's Center for Drug Evaluation and Research (CDER). “The FDA urges drug companies to ensure all drugs they make and market have appropriate FDA approval.”

The names of the products and the manufacturers and distributors that received the warning letters are:

* Codeine Sulfate Tablets, 30 mg, 60 mg – Lehigh Valley Technologies Inc., Allentown, Penn.
* Codeine Sulfate Tablets, 30 mg, 60 mg – Cerovene Inc., Valley Cottage, N.Y.
* Codeine Sulfate Tablets, 30 mg – Dava International Inc., Fort Lee, N.J.
* Codeine Sulfate Tablets, 30 mg, 60 mg – Glenmark Generics Inc. USA, Mahwah, N.J.

Companies receiving the warning letters have 15 days to give the FDA a plan to discontinue marketing the unapproved drugs. Manufacturers have 90 days to cease manufacturing of new product, and distributors have 180 days to cease further shipment of existing products. Previously manufactured unapproved products may still be found on pharmacy shelves for a period of time.

Today's action is part of the FDA's initiative against the marketing of unapproved drugs, announced in June 2006. At that time, the agency published a Compliance Policy Guide describing the FDA's risk-based enforcement approach to unapproved products.

“Doctors and patients often find that some drugs on the market do not have FDA approval,” said Deborah M. Autor, director of CDER's Office of Compliance. “This lack of approval undermines the FDA's process to ensure that safe and effective drugs are available to the U.S. public.”

Consumers who rely on opioid analgesics for pain relief have access to products that have been evaluated by the FDA and determined to be safe and effective for use. There are other FDA-approved drugs, including different opioid analgesics, which can be used to relieve pain. Consumers should consult a health care professional for detailed guidance on treatment options.

For additional information, including copies of the warning letters that identify the firms involved and the names of their products, see the FDA's Unapproved Drugs Web page/Enforcement Actions.

___________________________________________________________________________________________________________________________________________________________________________________________________________

musipedia org web site
http://www.musipedia.org/



snagfilms com web site
http://www.snagfilms.com/

Advisory re Band-Aid brand adhesive bandages identified as imported by Johnson&Johnson (Philippines), Inc.. which bears the following claim: "helps wounds
heal 2x faster". Has the Philippine FDA approved the use of said claim?
____________________________________________________________________________________________________________________________________________________________
Security lapses on October 13, 2009 at entrances to: SM Makati, Ace Hardware store, Park Square 1, all at Ayala Center, Makati. Because of said lapses,
I could have brought deadly weapons into said areas.

Advisory vs. JB Sports store, P-30 Park Square 1, Ayala Center, Makati.On October 13, 2009, said store sold to me a Voyage brand life vest without any visible (to unaided eye) name and address of the manufacturer/distributor
of said product. I believe said store violated the Consumer Act of the Philippines.


web site with useful, free information:


healthierus gov web site
http://www.healthierus.gov/

This Web site is part of a broad presidential agenda designed to help Americans, especially children, live longer, better, and healthier lives. The site
provides credible, accurate information to help Americans choose healthier habits.

The HealthierUS initiative is a national effort to prevent and reduce the costs of disease, improve people's lives and promote community health and
wellness.


www.smallstep.gov - Small Step for Adult & Teen

Small Steps make a big difference. Our small Steps program suggests some little things to make big changes in your life.



Senior Citizens' Resources
http://www.healthfinder.gov/search/?sort=date%253AD%253AL%253Ad1&output=xml&ie=UTF-8&client=healthfinder2&lr=lang_en&numgm=5&site=healthfnder&filter=0&q=senior+citizens

On October 7, 2009, the operator of SM Supermarket Makati, identified as Supervalue, Inc. East Drive, SM Makati Bldg. Ayala Center, San Lorenzao Village,
Makati City, sold to me what was identified as imported food product California Chips Honey BBQ potato chips which did not bear visible (to unaided eye)
address of the importer of said product. I believe said store violated the Consumer Act of the Philippines.

flu gov web site
http://www.flu.gov/

Get Smart: Know When Antibiotics Work
http://www.cdc.gov/Features/GetSmart/

Antibiotics do not fight infections caused by viruses, like colds, flu, most sore throats and bronchitis, and some ear infections. Rest, fluids, and over-the-counter products may be your or your child's best treatment option.
Dangers of Antibiotic Resistance

If antibiotics are used too often for things they can't treat—like colds, flu, or other viral infections—they can stop working effectively against bacteria when you or your child really needs them. Antibiotic resistance—when antibiotics can no longer cure bacterial infections—has been a concern for years and is considered one of the world's most pressing public health problems. Widespread overuse of antibiotics is fueling an increase in antibiotic-resistant bacteria. So the next time you or your child really needs an antibiotic for a bacterial infection, it may not work.

If You Have a Cold or Flu, Antibiotics Won't Work for You!

Colds and flu are caused by viruses, not bacteria. Taking antibiotics when you or your child has a virus may do more harm than good. Get smart about when antibiotics are appropriate—to fight bacterial infections. Taking them for viral infections, such as a cold, most sore throats, the flu, or acute bronchitis:

* Will not cure the infection;
* Will not keep other people from getting sick;
* Will not help you or your child feel better; and
* May cause unnecessary and harmful side effects.

What Not to Do

* Do not demand antibiotics when a healthcare provider says they are not needed.
* Do not take an antibiotic for a viral infection like a cold or most sore throats.
* Do not take antibiotics prescribed for someone else. The antibiotic may not be appropriate for your or your child’s illness. Taking the wrong medicine may delay correct treatment and allow bacteria to multiply.

If your healthcare provider prescribes an antibiotic for you or your child:

* Do not skip doses.
* Do not save any of the antibiotics for the next time you or your child gets sick.

What to Do

Snort, Sniffle, Sneeze.
View or download "Snort. Sniffle. Sneeze: No Antibiotics Please!" (video 3:47 mins) from

Learn about appropriate antibiotic use and how to feel better when you or your child has a sore throat, ear or sinus pain, fever, cough, or runny nose.

Adults and kids should clean their hands often, especially before meals and after touching pets. And make sure both you and your child are up-to-date on recommended immunizations.

Talk with your healthcare provider about the best treatment for your or your child’s illness. To feel better when you or your child has an upper respiratory infection:

* Increase fluid intake;
* Get plenty of rest;
* Use a cool-mist vaporizer or saline nasal spray to relieve congestion; and
* Soothe a throat with ice chips, sore throat spray, or lozenges (do not give lozenges to young children).

Video: Snort. Sniffle. Sneeze. No Antibiotics Please!

CDC created a video to help you learn more about appropriate antibiotic use and how to feel better when you or your child has a sore throat, ear or sinus
pain, fever, cough, or runny nose. This video features a doctor, who is also a concerned mom. You can download the video at CDC-TV, download the podcast
from http://www2a.cdc.gov/podcasts/player.asp?f=40102
or access on your mobile phone.



U.S. FDA Enforcement Report for Pctober 7, 2009
http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm185718.htm


Knowing How to Prevent Rabies isn't Just for Adults. Kids Can Get the Facts Too.
http://www.cdc.gov/Features/RabiesAndKids/
Rabies is a dangerous virus that is found in the saliva of animals. It can infect and kill animals and humans. Every 10 minutes, someone dies from rabies. Even though anyone can get rabies, more than half of the people who get rabies are kids under the age of 15. Now there's a rabies Web site that is just for kids – CDC Kids and Rabies

People usually get rabies when they are bitten by an animal that has the virus. When it's likely that you or a child is at serious risk for rabies, get help right away. Symptoms of rabies might not show up for months, but it is important to receive proper care very soon. When symptoms of rabies appear, people often die within a few days.

Early symptoms of rabies in people can include:

* fever
* headache
* weakness

As it gets worse, symptoms may include:

* difficulty sleeping
* anxiety
* confusion
* tingling sensation (usually at the site of the bite)
* excitation (being too excited)
* hallucinations (seeing things that aren't there)
* agitation
* salivating (drooling) more than usual
* difficulty swallowing
* fear of water

Below, you will learn about things you can do that will help make sure you never get rabies. Once you've read to the end, encourage a child to read through the information with you. Then visit the new Kids and Rabies Web site to learn more about rabies and to take a fun test of your rabies knowledge.
Help Your Pets Stay Rabies Free

Most people who have pets, such as dogs and cats, are very close to their animal companions. You might even have children and pets that are very close to each other. But there are times when pets are also in close contact with wild animals. If your pet is bitten by a wild animal that has rabies, your pet can get sick and die. It could also cause you or a child to get rabies from your sick pet.

When a human gets rabies, it's often because a pet got rabies first. The good news is that there are things children and adults alike can do to help make sure your pets never get rabies. That way, they will stay healthy and won't cause humans to get rabies.

Things you should do include:

* Take your pets to a veterinarian on a regular basis. They will keep your pets up-to-date on their rabies shots, which helps protect them from rabies.
* Talk to your veterinarian about spaying or neutering your pet. This helps cut down on the number of stray animals.
* Call animal control to remove all stray animals from your neighborhood. These animals may not have gotten their rabies shot and can give other animals and people rabies.
* Remind kids not to go near stray animals and remind them to tell an adult if they see a pet wandering around without any person watching them closely.
* Keep your pets indoors. When a dog goes outside, make sure an adult is there to watch it and keep it safe. Make sure children know not to take their pet outside without an adult around.
* Do not feed or put water for your pets outside. Keep your garbage covered. These items may cause wild animals to come near your yard or house.

Stay Away From Wild Animals

Most of the time, rabies is found in wild animals. The main animals that get rabies include raccoons, skunks, foxes and bats.

If you see a wild animal acting strangely, stay away from it. Help kids to understand that they should avoid wild animals at all times. Some things to look for are:

* General sickness
* Problems swallowing
* Lots of drool or saliva
* An animal that appears more tame than you would expect
* An animal that bites at everything
* An animal that's having trouble moving or may even be paralyzed

Animals that act this way may need to be helped by people who know how to take care of wild animals. Call animal control and make sure the animal gets the help it needs.

Sometimes, people may come across a dead animal. Never pick up or touch dead animals and make sure children know to stay away from dead animals. Animals who have died can still give people rabies, especially if they have only been dead for a short time. If a dead animal is spotted, call animal control to properly take care of the animal's body.

Get Help If An Animal Bites You

Animals can sometimes bite people even when you try to avoid them. If an animal bites you, seek help immediately. Let kids know that they should tell an adult immediately if they are bitten by an animal. Show them how to wash with soap and water so that they will know what to do if they are bitten. They should then be taken to a doctor who will know what to do next.

Most of the time, people know when an animal bites them. But that's not always the case with bats, which are one of the main animals that can give you rabies. Bats have small teeth that might not always be felt when they bite and they don't always leave bite marks that are easily seen.

Bats can be found indoors or out. Make sure children know to tell an adult when:

* a bat comes near or touches them
* a bat flies into their room or place where they sleep
* they find a dead bat
* they hear others talk about touching a living or dead bat

Visit CDC's Kids and Rabies Web Site

Now there's a rabies Web site that is just for kids – CDC Kids and Rabies.

This is where children can learn more about how rabies affects animals and humans and get more tips on how to prevent rabies.

The website features an interactive quiz and e-cards, buttons, and badges that can be sent to family and friends so they can learn about rabies too.

NOTE: If you've read this website, you have all the information you need to ace the quiz. So, take the quiz by yourself or with your child and share the information so you can help protect others from getting rabies.




Make It Easier to Control Your Weight
http://newsinhealth.nih.gov/2009/October/feature1.htmOn the face of it, controlling your weight is simple: eat less and exercise more. But it’s much harder than it sounds. Researchers have recently found several factors influencing your weight that you might not be aware of. Here’s how to recognize and take control of the things that may be tripping up your efforts at weight control.



You probably have a pretty good idea what a healthy diet is. Unfortunately, studies show that Americans are not eating enough fruits, vegetables and whole grains. And we’re eating too much fat and salt. So where are we going wrong?

Part of the problem, according to Dr. Andrew Rundle of Columbia University, is that so many things around us influence the seemingly simple balance between how many calories we eat and how many we burn. “I’ve often thought that the obesity epidemic is an epidemic of a thousand paper cuts,” he says. “So many things prod us throughout the day to raise our calorie intake and lower our energy expenditure.”

Once you recognize what these things are, you can take control of your surroundings to make healthy habits easier.

First off, learn how to read nutrition labels and ignore the rest of the packaging. Phrases like “low-fat” don’t necessarily mean anything if you’re concerned about calories. Some low-fat and non-fat foods actually have more calories than the normal versions.

“It’s not enough just to have the perception that something’s healthy,” says Dr. Susan Yanovski, co-director of the Office of Obesity Research at NIH’s National Institute of Diabetes and Digestive and Kidney Diseases. “You actually have to look at what’s in it.”

Make sure to look at the number of portions, too, she says. That muffin might seem like it has 150 calories, but if the serving size is 1/3 of a muffin, it really has 450 calories.

Did you know that the size and shape of what’s holding your food can affect how much you eat? “People basically eat what’s put in front of them,” Yanovski says. It’s the amount of food you eat that counts, not what it looks like. So try serving food on smaller plates and bowls if you’d like to eat less.

One of the reasons eating out has become such a challenge is that restaurant food portions have gotten larger. Super-sized dishes may seem like a good value, but not if they get you to eat more than your body needs. Order smaller dishes and plan to share larger ones. Or set aside a portion to take home with you before you even put a bite in your mouth.

It’s easy to fool yourself about how much you’re eating—and, it turns out, about how healthy the food is. Marketing researchers have found that when restaurants claim to be healthy, people are more likely to underestimate the calories in their main dish and order higher calorie side dishes. One study found that when there’s healthy food available, people actually make more indulgent choices. Remember, it’s what you eat that counts, not what you think about eating.

Some areas have enacted laws requiring restaurants to list calories on the menu. “When people actually have calorie values staring them in the face, they may make better choices,” Yanovski says.

Unfortunately, in most places, you have to do some work to check calories when you eat out. Some restaurants may have nutrition information available if you request it, or might have it posted on their web site.

You may not think about sleep when you’re concerned with weight, but studies show that people who get less sleep have a higher risk of obesity (along with other health problems). Lack of sleep can disrupt the normal chemical signals in your body and lead you to eat more. So try to get enough sleep. And make sure not to snack mindlessly when you’re sleepy, like late at night.

Your neighborhood and community can affect your weight as well. A research team led by Rundle found that access to produce markets, supermarkets and health food stores is associated with lower rates of obesity in New York City.

“It’s also an issue in rural areas because the very small towns don’t have supermarkets,” says Dr. Madeline Dalton of Dartmouth Medical School. “Sometimes you need to drive 15 to 20 miles to get to a store that has fruits and vegetables. Clearly, that’s a problem.”

Wherever you live, Dalton says, you need to plan to eat well. “It’s really a matter of getting to know your environment and figuring out how to get healthy food on a regular basis.”

Your surroundings can also affect how active you are. Studies show that people in neighborhoods without sidewalks, or who live far from a recreational facility or a walking or biking trail, are more likely to be obese. People who perceive their community as unpleasant or unsafe are also more likely to be obese. Recognize your particular challenges and figure out how to add exercise and physical activity to your daily routine.

Once you identify the things that affect your weight, you can start changing them. Set modest goals and gradually improve your habits. “Pick 1 or 2 things in your life that you think you can change,” Dalton says. “Just walk a quarter of a mile a day to get started. Cut out 1 soda every day.” You may have to try a few times, but when you meet each goal you can move on to the next one.

NIH-funded research has found that people who are close influence each other’s weight. You may be more likely to lose weight if you work with friends, relatives and co-workers to develop healthier lifestyles. Get the family together to make nutritious meals. Form walking groups with co-workers. Take a dance class with friends.

“What you really want to do is make the healthy choice the easy choice, the default choice,” Yanovski says.

Definitions

Calories
The amount of energy stored in food. When you eat more calories than your body can use, it stores that extra energy as fat.

Wise Choices iconWise Choices

Weight Control Tips

* Use nutrition labels. Don’t guess how many calories you’re eating.
* Watch your portions. Value-size servings aren’t a bargain if you’re eating too much.
* Cut the sugar. Don’t let sugary soda or other sweets crowd out healthy foods and drinks.
* Don’t eat out of habit. Mindless eating at work or in front of the TV can pack on the pounds.
* Think about the whole meal, not just the main course.
* Use smaller dishes and containers. Larger ones encourage you to eat more.
* Keep reminders of how much you’re eating. Wrappers, empty containers and bones nearby remind you of how much you’ve eaten.
* Get enough sleep. Less sleep is linked to higher rates of obesity.
* Get active. Look for opportunities to add physical activity to your daily routine.
* Do it together. Family, friends and coworkers can all help each other make healthy changes to their lives.



Protect Your Property or Business from Disaster
http://www.fema.gov/plan/prevent/howto/index.shtm

web site with useful, free information:

US cert gov web site

Cyber Security Tips

Cyber Security Tips describe and offer advice about common security issues for non-technical computer users.

Sign up to receive these security tips in your inbox.


tips RSS feed Add to My Yahoo!

General information

* Why is Cyber Security a Problem?
* Guidelines for Publishing Information Online
* Understanding Internet Service Providers (ISPs)

General security

* Choosing and Protecting Passwords
* Understanding Anti-Virus Software
* Understanding Firewalls
* Coordinating Virus and Spyware Defense
* Debunking Some Common Myths
* Good Security Habits
* Safeguarding Your Data
* Real-World Warnings Keep You Safe Online
* Keeping Children Safe Online

Attacks and threats

* Dealing with Cyberbullies
* Understanding Hidden Threats: Corrupted Software Files
* Understanding Hidden Threats: Rootkits and Botnets
* Preventing and Responding to Identity Theft
* Recovering from Viruses, Worms, and Trojan Horses
* Recognizing and Avoiding Spyware
* Avoiding Social Engineering and Phishing Attacks
* Understanding Denial-of-Service Attacks
* Identifying Hoaxes and Urban Legends
* Avoiding the Pitfalls of Online Trading

Email and communication

* Understanding Your Computer: Email Clients
* Using Caution with Email Attachments
* Reducing Spam
* Benefits and Risks of Free Email Services
* Benefits of Blind Carbon Copy (BCC)
* Understanding Digital Signatures
* Using Instant Messaging and Chat Rooms Safely
* Staying Safe on Social Network Sites

Mobile devices

* Protecting Portable Devices: Physical Security
* Protecting Portable Devices: Data Security
* Using Caution with USB Drives
* Securing Wireless Networks
* Cybersecurity for Electronic Devices
* Defending Cell Phones and PDAs Against Attack

Privacy

* How Anonymous Are You?
* Protecting Your Privacy
* Understanding Encryption
* Effectively Erasing Files
* Supplementing Passwords

Safe browsing

* Understanding Your Computer: Web Browsers
* Evaluating Your Web Browser's Security Settings
* Shopping Safely Online
* Browsing Safely: Understanding Active Content and Cookies
* Understanding Web Site Certificates
* Understanding Internationalized Domain Names
* Understanding Bluetooth Technology
* Avoiding Copyright Infringement

Software and applications

* Understanding Patches
* Understanding Voice over Internet Protocol (VoIP)
* Risks of File-Sharing Technology
* Reviewing End-User License Agreements
* Understanding Your Computer: Operating Systems



FDA Orders Postmarket Surveillance Studies on Certain Spinal Systems
Tuesday, October 6, 2009 4:07 AM
From:
"U.S. Food & Drug Administration (FDA)"


FDA Orders Postmarket Surveillance Studies on Certain Spinal Systems
Mon, 05 Oct 2009 15:53:00 -0500

The U.S. Food and Drug Administration today ordered manufacturers of certain types of pedicle screw systems, called dynamic stabilization systems, to
conduct postmarket surveillance studies to collect clinical data on a number of potential safety issues, including fusion rates and frequency of additional
surgeries.

Recognize and Prevent MRSA Infections
http://www.cdc.gov/Features/MRSAInfections/

Advisory for potential customers of LBC delivery service:
For your own protection, before availing of said delivery service, demand a statement, in writing,from said company, that it will provide you with proof in writing that any package you send through said company has been received by the addressee.



Re Senator Loren Legarda.
According to a source, identified as columnist Ching M. Alano, Senator Loren Legarda has come up with her own prayer: "It goes something like this: "Dear Lord, in
addition to the prayers going around - of petitions that you hold Pepeng by your mighty hands - we pray that we learn to protect Mother Nature from now on. That we will each plant and nurture five trees or more a year; that we reduce, recycle and reuse; and know that you are God."




FDA Patient Safety News
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/psn/index.cfm

New Colchicine Product and Dosing Regimen (Video, print, and e-mail functions)

FDA has approved the first single-ingredient oral colchicine product. The drug, called Colcrys, is approved to treat acute gout flares and familial Mediterranean fever. Oral colchicine has been used to treat gout in the past, but until now it had not been approved by FDA.

Colchicine has historically been given every hour for acute gout flares, either until the flare subsided or treatment had to be stopped because the patient developed gastrointestinal problems. But a dosing study conducted as part of the approval of Colcrys demonstrated that one initial dose and a single additional dose after one hour was just as effective and much less toxic. Healthcare professionals should use this lower recommended dosing regimen to treat acute gout flares.

Healthcare professionals should also be aware that colchicine interacts with other drugs, including P-glycoprotein and strong CYP3A4 inhibitors such as cyclosporine and clarithromycin. This can lead to serious or even fatal colchicine toxicity, particularly if a patient has renal or hepatic impairment. And so concomitant use of colchicine and P-glycoprotein or strong CYP3A4 inhibitors is contraindicated in these patients. For patients with normal renal and hepatic function, consider interrupting colchicine therapy or reducing the dose if the patient needs treatment with a P-glycoprotein or a strong CYP3A4 inhibitor.

Additional Information:

* FDA MedWatch Safety Alert. Colchicine (marketed as Colcrys). July 30, 2009.
* FDA Press Release. FDA Approves Colchicine for Acute Gout, Mediterranean Fever. July 30, 2009.


Potentially Fatal Errors with Certain Glucose Test Strips
FDA Patient Safety News: Show #91, October 2009

FDA is warning again that potentially fatal glucose monitoring errors can occur in patients who receive therapeutic products containing certain sugars other than glucose. These products include oral xylose, intravenous infusions that contain maltose or galactose, and peritoneal dialysis solutions that contain icodextrin, such as Extraneal. A more specific product list can be found below.

The problem is that some glucose meters use a type of test strip (GDH-PQQ) that cannot distinguish between glucose and these other sugars, so the reading on one of these test strips will reflect both the patient's actual blood glucose and the other sugar the patient received. These falsely elevated readings can mask significant hypoglycemia, or they can lead to excessive insulin administration. This can result in severe hypoglycemia, coma and death. Other glucose test strip methodologies are not affected by the presence of non-glucose sugars.

FDA has received 13 reports of deaths associated with GDH-PQQ test strips that had documented interference from maltose or other non-glucose sugars. The deaths occurred in healthcare facilities. Ten of the 13 patients were receiving Extraneal peritoneal dialysis solution for renal failure. Three of the 13 patients were receiving maltose-containing substances. Patients were treated with insulin doses or insulin drips that were guided by falsely elevated blood sugar results. Six of the 13 deaths have occurred since 2008, despite previous warnings from FDA and others.

FDA is now recommending that healthcare facilities avoid using GDH-PQQ glucose test strips, which include several types of ACCU-CHEK, TRUEtest and Freestyle test strips.

If a facility does use GDH-PQQ test strips, FDA recommends additional precautions:

• Determine whether patients are receiving products that contain other sugars when they are admitted and periodically during their stay at the facility.

• If patients are receiving one of these interfering products, never use GDH-PQQ test strips to monitor their blood glucose. Instead, use only laboratory-based glucose assays. This also holds true for patients who are unresponsive or cannot communicate adequately.

• Educate the staff about this potentially fatal problem, and consider safeguards such as drug interaction alerts in computer order entry systems, patient profiles and charts. And for patients who are not receiving interfering products, periodically verify glucose meter readings with laboratory-based results.

FDA is working with glucose monitoring manufacturers to address problems with GDH-PQQ glucose test strips, and will continue to monitor adverse events associated with these products.

Additional Information:

FDA MedWatch Safety Alert. GDH-PQQ (glucose dehydrogenase pyrroloquinoline quinone) Glucose Monitoring Technology. August 13, 2009.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm177295.htm
FDA Patient Safety News is available at www.fda.gov/psn


Certain Lots of Teva Propofol Recalled
FDA Patient Safety News: Show #91, October 2009

Teva Pharmaceuticals is recalling certain lots of Propofol Injectable Emulsion 10 mg/mL because some of the vials in these lots contain elevated endotoxin levels.

The company says that it has received over 40 reports of patients treated with propofol who experienced fever, chills and other flu-like symptoms post-operatively. Based on available information, these febrile or flu-like reactions were self-limited and spontaneously resolved. However, patients exposed to high endotoxin levels could experience serious adverse effects, such as disseminated intravascular coagulopathy, acute respiratory distress syndrome, shock, and death.

The recall affects lot numbers 31305429B and 31305430B, which contain 100 mL vials. Anyone with propofol from these lots should not use it and return it to the distributor. For more information, contact Teva Pharmaceuticals at 1-866-262-1243.

Additional Information:

FDA MedWatch Safety Alert. Propofol Injectable Emulsion, 10 mg/mL 100 mL vials. July 16, 2009.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm172507.htm
FDA Patient Safety News is available at www.fda.gov/psn

Alaris (Medley) Infusion Systems Recalled
FDA Patient Safety News: Show #91, October 2009

CareFusion is alerting healthcare professionals about a number of safety problems with several models of Alaris infusion systems. These problems could cause patients to be over or under-infused, which could lead to serious injury or death.

Certain units of the following Alaris devices are affected:

• Point-of-care Units, Models 8000 and 8015

• Pump Module, Model 8100

• Patient-Controlled Analgesia Module, Model 8120

• Inter-Unit Interface Connectors for the Alaris System

These devices were formerly sold under the "Medley" name.

The company notified customers about these potential problems in June, and described its plans to provide software and hardware corrections over the next several months. Until then the company's notice advises pump users to take certain steps to mitigate the problems.

For example, one failure can affect the Alaris PC unit when it is used with the PCA module. The pump is supposed to verify that the volume of medication in the syringe will deliver the infusion that is programmed. But if the infusion rate exceeds the volume of therapy in the syringe, a warning is displayed. If the pump user confirms the infusion and the patient presses the button on his handset to deliver medication, the pump may deliver the entire contents of the syringe to the patient, which could cause serious injury or death.

The company says that if the syringe volume warning appears, you must first take the dose request handset from patients to keep them from pressing the button. Then, press the “CONFIRM” key, then the “PAUSE” key to halt the infusion. Remove the syringe, verify the concentration, and reprogram the infusion. Do not return the handset to the patient until you have reprogrammed the infusion and confirmed that it's been programmed properly.

Another example involves the possible failure of the circuitry that protects against electrostatic discharge in certain Alaris PC units. Because of this, there could be problems with the entry keypad, including the possibility that the keypad could not respond to key presses, or that key entries could register incorrectly or could occur without keys being pressed. Pump users should always verify the drug name, concentration, and programmed infusion parameters before starting an infusion. If a keypad does not perform correctly, take the pump out of service and return it to the company.

You can get more information about the Alaris System recall by calling the CareFusion recall center at 888-562-6018.

Additional Information:

FDA MedWatch Safety Alert. Alaris System (Cardinal Health). August 5, 2009.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm174797.htm

Cardinal Health/CareFusion Customer Letter. Urgent: Medical Device Recall Notification – Update to Previous Recall Information. July 29, 2009.
http://www.carefusion.com/Images/Recall_Update_29July2009_tcm10-5320.pdf

Cardinal Health Customer Letter. Urgent: Medical Device Recall Notification. June 12, 2009.
http://www.carefusion.com/Images/CustomerLetter-Signed_tcm10-5325.pdf
FDA Patient Safety News is available at www.fda.gov/psn


Recall of Certain Hospira Devices
FDA Patient Safety News: Show #91, October 2009

Hospira, Inc. has issued an alert about a number of the company's medical devices that have defective AC power cords. These devices include infusion pumps, compounders, monitoring devices and printers.

This action comes after reports of sparking, charring and fires on the plug of the power cord. Hospira has determined that the power cord's prongs may crack and fail at or inside the plug. That could lead to fire, electrical shock, device failure, and interference with therapy. Depending on the device and the type of therapy, these failures could cause potentially serious injury or death.

Hospira is working with its customers to replace the power cords on all the affected devices, regardless of their condition. The complete list of these devices can be found below.

In the meantime, Hospira is advising users of the affected devices to inspect their power cords. The defective cords have a prong and ground-pin insert design, with a black plastic bridge connecting the terminal prongs on the plug. Devices with power cords that don't have this black bridge connecting the terminal prongs are not affected.

Anyone who finds a cord with bent or cracked prongs, burnt plastic, or excessive wear and tear should immediately stop using the device and contact Hospira to find out how to get replacement parts or devices. The company can be contacted at 1-800-241-4002. Power cords that don't show any of these potentially dangerous characteristics should be monitored regularly until they can be replaced.

Additional Information:

Hospira Press Release. Hospira Issues Urgent Device Recall For AC Power Cords. August 14, 2009.
http://www.fda.gov/Safety/Recalls/ucm178158.htm
FDA Patient Safety News is available at www.fda.gov/psn


“Nuby” Gel-filled Teethers Recalled
FDA Patient Safety News: Show #91, October 2009

Parents and other caregivers of small children should be aware that the company Luv N' Care Ltd. has recalled almost 20 styles of gel-filled teethers because they might be contaminated with bacteria.

The gel inside these teethers may contain Bacillus subtilis and Bacillus circulans. Adults exposed to these bacteria generally do not get sick. However, if the teether is punctured and infants or children with weakened immune systems ingest the gel containing these bacteria, they could suffer stomach pain, vomiting, diarrhea, and occasionally more serious disease.

The recall affects 15 styles of gel-filled teethers sold under the brand name "Nuby", two sold under the "Cottontails" name and one sold under the "Playskool" name. UPC codes for these styles can be found below. Consumers who have these teethers should stop using them immediately and either throw them away or return them to the place of purchase for a refund. For questions, contact the company at 1-800-256-2399, ext. 3106.

Additional Information:

FDA MedWatch Safety Alert. Nuby Gel Filled, Cottontails, and Playskool Teethers. August 12, 2009.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm172712.htm
FDA Patient Safety News is available at www.fda.gov/psn



U.S. Department of Health & Human Services National Institutes of Health Research Matters
http://www.nih.gov/news/research_matters/index.htm

NIH Research Matters is a review of NIH research from the Office of Communications and Public Liaison, Office of the Director, National Institutes of Health.

Cocaine Vaccine Shows Promise for Treating Addiction
http://www.nih.gov/news/health/oct2009/nida-05.htm


Embargoed for Release
Monday, October 5, 2009
4:00 p.m. EDT

Cocaine Vaccine Shows Promise for Treating Addiction
NIDA Study Suggests Harnessing the Immune System Against Cocaine Addiction May Prove Effective

Immunization with an experimental anti-cocaine vaccine resulted in a substantial reduction in cocaine use in 38 percent of vaccinated patients in a clinical trial supported by the National Institute on Drug Abuse (NIDA), a component of the National Institutes of Health. The study, published in the October issue of the Archives of General Psychiatry, is the first successful, placebo-controlled demonstration of a vaccine against an illicit drug of abuse.

"The results of this study represent a promising step toward an effective medical treatment for cocaine addiction," said NIDA Director Dr. Nora Volkow." Provided that larger follow-up studies confirm its safety and efficacy, this vaccine would offer a valuable new approach to treating cocaine addiction, for which no FDA-approved medication is currently available."

Like vaccines against infectious diseases such as measles and influenza, the anti-cocaine vaccine stimulates the immune system to produce antibodies. Unlike antibodies against infectious diseases, which destroy or deactivate the disease-causing agents, anti-cocaine antibodies attach themselves to cocaine molecules in the blood, preventing them from passing through the blood-brain barrier. By preventing the drug’s entry into the brain, the vaccine inhibits or blocks the cocaine-induced euphoria.

This study included 115 patients from a methadone maintenance program who were randomly assigned to receive the anti-cocaine vaccine or a placebo (inactive) vaccine. Participants were recruited from a methadone maintenance program because their retention rates are substantially better than programs focused primarily on treatment for cocaine abuse. Participants in both groups received five vaccinations over a 12-week period and were followed for an additional 12 weeks. All participants also took part in weekly relapse-prevention therapy sessions with a trained substance abuse counselor, had their blood tested for antibodies to cocaine, and had their urine tested three times a week for the presence of opioids and cocaine.

Participants differed in the levels of antibodies generated in response to vaccination. Thirty-eight percent attained blood levels of anti-cocaine antibodies thought to be sufficient to block cocaine's euphoric effects. During weeks 9 to 16 (when antibody levels peaked), these participants had significantly more cocaine-free urines than those who received the placebo or those with active vaccine but low levels of anti-cocaine antibodies. Participants with the highest antibody levels had the greatest reductions in cocaine use. No serious adverse effects were associated with vaccine treatment.

"Fifty-three percent of participants in the high-antibody group were abstinent from cocaine more than half the time during weeks 8 to 20, compared with only 23 percent of participants with lower levels of antibodies," said Thomas Kosten, M.D., of Baylor College of Medicine in Houston, the study's principal investigator.

"In this study immunization did not achieve complete abstinence from cocaine use," added Dr. Kosten. "Previous research has shown, however, that a reduction in use is associated with a significant improvement in cocaine abusers’ social functioning and thus is therapeutically meaningful."

Dr. Kosten led the study in collaboration with colleagues from Yale University School of Medicine, the Connecticut Veterans Administration (VA) Healthcare System, Baylor College of Medicine, and the Michael E. DeBakey VA Medical Center.




FDA Orders Postmarket Surveillance Studies on Certain Spinal Systems
Tuesday, October 6, 2009 4:07 AM
From:
"U.S. Food & Drug Administration (FDA)"


FDA Orders Postmarket Surveillance Studies on Certain Spinal Systems
Mon, 05 Oct 2009 15:53:00 -0500

The U.S. Food and Drug Administration today ordered manufacturers of certain types of pedicle screw systems, called dynamic stabilization systems, to conduct postmarket surveillance studies to collect clinical data on a number of potential safety issues, including fusion rates and frequency of additional surgeries.


U.S. ATTORNEY NEWS RELEASE: VEAL COMPANY CHARGED IN CASE OF TAINTED FEED
http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm185288.htm
Wed, 30 Sep 2009 00:00:00 -0500

United States Attorney Michael L. Levy today announced the filing of an Information1 against Select Veal Feeds, Inc., and its owner Wayne A. Marcho, charging the defendants with one count of misbranding, in violation of the Food, Drug and Cosmetic Act. The charge arises from the shipment of formaldehyde and potassium permanganate, between 1998 through 2005, which the defendants directed their contract farmers to use as part of the veal calves’ feeding routine. Defendant Select Veal Feeds, Inc. is also charged with one count of obstructing an agency proceeding based on false statements to inspectors from the Food and Drug Administration (“FDA”) in January 2004.


For a copy of the news release, visit the U.S. Attorney's web site.



US cert gov web site

Cyber Security Tips

Cyber Security Tips describe and offer advice about common security issues for non-technical computer users.

Sign up to receive these security tips in your inbox.


tips RSS feed Add to My Yahoo!

General information

* Why is Cyber Security a Problem?
* Guidelines for Publishing Information Online
* Understanding Internet Service Providers (ISPs)

General security

* Choosing and Protecting Passwords
* Understanding Anti-Virus Software
* Understanding Firewalls
* Coordinating Virus and Spyware Defense
* Debunking Some Common Myths
* Good Security Habits
* Safeguarding Your Data
* Real-World Warnings Keep You Safe Online
* Keeping Children Safe Online

Attacks and threats

* Dealing with Cyberbullies
* Understanding Hidden Threats: Corrupted Software Files
* Understanding Hidden Threats: Rootkits and Botnets
* Preventing and Responding to Identity Theft
* Recovering from Viruses, Worms, and Trojan Horses
* Recognizing and Avoiding Spyware
* Avoiding Social Engineering and Phishing Attacks
* Understanding Denial-of-Service Attacks
* Identifying Hoaxes and Urban Legends
* Avoiding the Pitfalls of Online Trading

Email and communication

* Understanding Your Computer: Email Clients
* Using Caution with Email Attachments
* Reducing Spam
* Benefits and Risks of Free Email Services
* Benefits of Blind Carbon Copy (BCC)
* Understanding Digital Signatures
* Using Instant Messaging and Chat Rooms Safely
* Staying Safe on Social Network Sites

Mobile devices

* Protecting Portable Devices: Physical Security
* Protecting Portable Devices: Data Security
* Using Caution with USB Drives
* Securing Wireless Networks
* Cybersecurity for Electronic Devices
* Defending Cell Phones and PDAs Against Attack

Privacy

* How Anonymous Are You?
* Protecting Your Privacy
* Understanding Encryption
* Effectively Erasing Files
* Supplementing Passwords

Safe browsing

* Understanding Your Computer: Web Browsers
* Evaluating Your Web Browser's Security Settings
* Shopping Safely Online
* Browsing Safely: Understanding Active Content and Cookies
* Understanding Web Site Certificates
* Understanding Internationalized Domain Names
* Understanding Bluetooth Technology
* Avoiding Copyright Infringement

Software and applications

* Understanding Patches
* Understanding Voice over Internet Protocol (VoIP)
* Risks of File-Sharing Technology
* Reviewing End-User License Agreements
* Understanding Your Computer: Operating Systems


Welcome to the US-CERT Mailing List Subscription System

Four mailing lists are available, choose the ones most suited to your interests:

* Technical Cyber Security Alerts -Written for system administrators and experienced users, technical alerts provide timely information about current security issues, vulnerabilities, and exploits. View all of the technical cyber security alerts.

* Cyber Security Bulletins -Bulletins summarize information that has been published about new security issues and vulnerabilities for the week prior. They are published weekly and are written primarily for system administrators and other technical users. View all of the cyber security bulletins.

* Cyber Security Alerts - Written for home, corporate, and new users, these alerts are published in conjunction with technical alerts when there are security issues that affect the general public. View all of the cyber security alerts.

* Cyber Security Tips - Tips provide information and advice about a variety of common security topics. They are published every two weeks and are written primarily for home, corporate, and new users. View all of the cyber security tips.

* Current Activity Updates - Provide up-to-date information about high-impact types of security activity affecting the community at large. Current activity is updated on an as needed basis which ranges from several times a week, to several times a day. Subscribers can expect to receive one update- per entry- as they are published to the US-CERT website. View the recent current activity updates.

safety tips after a flood

Safety Tips After a Flood
Source: MERALCO

After a flood hits your home, be very cautious before you power up, plug and turn on your
appliances.


Check if your house is the only one without power or if it's the whole neighborhood. If your
home is the only one without power, you need to check your home electrical system. Ask a
competent licensed electrician to do this for you.

Please remember these helpful safety remiders:

* Make sure that the main electrical switch or circuit breaker is turned off.

* Unplug all equipment and appliances. Turn off switches of permanently connected
equipment. Unscrew all light bulbs if possible.

* Remove mud and and dirt from the service equipment or main circuit breaker/fuse and its enclosure, using protective gear or equipment such as rubber gloves, rubber soled shoes and well insulated pliers.



* As a safety precaution, always assume the wires are "hot," "live" or energized whenever working.


* Allow convenience outlets, switches, electrical wires, sockets, connectors, breakers and other devices to dry completely. Drying may take days, depending on how wet the system is and on the external temperature.



* When all electrical wires and accessories are dry and clean, proper testing must be done to ensure the integrity of the electrical system.


* Appliances must be completely dry and serviced or checked by a licensed electrician or service center agent.

Do not turn on damaged electrical appliances.

* Be observant and watchful after powering up your house to immediately detect any
abnormalities.

IMPORTANT REMINDER: If your electric meter was submerged in water, please report this to the Meralco hotline number 16211 or text to 0917-559-2824 or 0920-929-2824. You may also call the Meralco hotline number if you need the services of a licensed electrician.




CDC H1N1 Flu Website Situation Update October 2 2009
H1N1 Flu Vaccine Information Statements (VISs)

Vaccine Information Statements (VISs) are information sheets produced by CDC that explain to vaccine recipients, their parents, or their legal representatives both the benefits and risks of a vaccine.

* Inactivated 2009 H1N1 Influenza Vaccine Adobe PDF file
(the flu shot)
http://www.cdc.gov/vaccines/pubs/vis/downloads/vis-inact-h1n1.pdf

* Live, Intranasal 2009 H1N1 Influenza Vaccine Adobe PDF file
(the nasal spray vaccine)
http://www.cdc.gov/vaccines/pubs/vis/downloads/vis-laiv-h1n1.pdf


What's New on the FDA Drugs Site

October 2, 2009

New and Generic Drug Approvals

October 2, 2009

* Alfuzosin Hydrochloride Extended-Release Tablets, Wockhardt, Ltd., Tentative Approval
* Carbidopa and Levodopa Tablets, Mylan Pharmaceuticals, Inc., Approval
* Cilostazol Tablets, Breckenridge Pharmaceutical, Inc., Approval
* Cordarone (amiodarone hydrochloride) Tablets, Wyeth Pharmaceuticals, Inc., Labeling Revision
* DepoDur (morphine sulfate) Liposome Injection, Pacira Pharmaceuticals, Inc., Labeling Revision
* Invega Sustenna (paliperidone palmitate) Extended-Release Intramusculuar Suspension, Ortho-McNeil-Jansen Pharmaceuticals, Inc., Approval
* Kayexalate (sodium polystyrene sulfonate) Oral or Rectal Powder, sanofi-aventis U.S., LLC, Labeling Revision
* Lithium Carbonate Capsules, InvaGen Pharmaceuticals, Inc., Approval
* Maxipime (cefepime hydrochloride) Injection, Bristol-Myers Squibb Co., Labeling Revision
* Metoprolol Tartrate Injection, Luitpold Pharmaceuticals, Inc., Approval
* Ondansetron Hydrochloride Injection, Gland Pharma, Ltd., Approval
* Oxaliplatin Injection, Hospira Worldwide, Inc., Approval
* Renvela (sevelamer carbonate) Oral Suspension, Genzyme Corp., Approval
* Stelara (ustekinumab) Injection, Centocor Ortho Biotech, Inc., Approval
* Zoledronic Acid Injection, Bedford Laboratories, Tentative Approval


happynews com web site
http://www.happynews.com/

CDC H1N1 Flu Website Situation Update October 2 2009
H1N1 Flu Vaccine Information Statements (VISs)

Vaccine Information Statements (VISs) are information sheets produced by CDC that explain to vaccine recipients, their parents, or their legal representatives both the benefits and risks of a vaccine.

* Inactivated 2009 H1N1 Influenza Vaccine Adobe PDF file
(the flu shot)
http://www.cdc.gov/vaccines/pubs/vis/downloads/vis-inact-h1n1.pdf

* Live, Intranasal 2009 H1N1 Influenza Vaccine Adobe PDF file
(the nasal spray vaccine)
http://www.cdc.gov/vaccines/pubs/vis/downloads/vis-laiv-h1n1.pdf


essentials of music web site
http://www.essentialsofmusic.com/



Philips Issues Worldwide Recall of Select Heartstart Fr2+ Automated External Defibrillators
http://www.fda.gov/Safety/Recalls/ucm185108.htm








Philips Issues Worldwide Recall of Select Heartstart Fr2+ Automated External Defibrillators





FOR IMMEDIATE RELEASE - September 28, 2009 - Seattle - Philips announced today that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a memory chip failure that may render the device inoperable. Only certain HeartStart FR2+ AEDs (models M3860A and M3861A, distributed by Philips; and models M3840A and M3841A, distributed by Laerdal Medical) manufactured between May, 2007 and January, 2008 are included in the voluntary recall.

The HeartStart FR2+ defibrillators are used by trained responders and designated response teams to help treat sudden cardiac arrest. The device automatically analyzes the heart rhythm and determines whether a defibrillation shock is needed. If a shockable rhythm is detected, the FR2+ instructs the responder to deliver defibrillation therapy.

Philips has received reports of a memory chip failure in a small number of FR2+ units manufactured in 2007 and early 2008. These reported failures were detected during routine self tests, not during emergency use of the AED. Failure of this chip could render the AED inoperable and prevent it from delivering therapy when indicated, although Philips has received no reports of injury associated with this chip failure.

The AEDs affected by this recall have been distributed globally to fire departments, emergency medical services, hospitals, and other organizations. Philips is contacting customers to arrange for the return and replacement of all the recalled AEDs by sending notification letters to distributors and users. In addition, the company has set up a page on the Philips Web site with a serial number look-up tool to allow customers to find out if their FR2+ is part of this recall, as well as instructions on what to do if it is. The Web page is www.philips.com/FR2PlusAction.

Philips has notified the U.S. Food & Drug Administration (FDA) of its decision to voluntarily recall the affected product. Customers who have questions about the recall or wish to report product problems may contact HeartStart Customer Service at 1-800-263-3342.

Any adverse events experienced with the use of this product should be reported to the FDA’s MedWatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch Web site at www.fda.gov/medwatch.



RSS Feed for FDA Recalls Information

-
-

Page Last Updated: 10/03/2009



On October 4, 2009, Robinsons Supermarket Ermita sold a food product without a visible
(to unaided eye) best before date.