Showing posts with label Benadryl. Show all posts
Showing posts with label Benadryl. Show all posts

Saturday, May 1, 2010

Another Recall for Tylenol and other medicines

UPDATE: 5 May -
FDA found bacteria in lots for recalled Tylenol
By MATTHEW PERRONE, AP Business Writer

WASHINGTON – Ingredients used by Johnson & Johnson in some of the 40 varieties of children's cold medicines recalled last week were contaminated with bacteria, according to a report by the Food and Drug Administration.

Agency officials said Tuesday none of the company's finished products tested positive for the contaminants, though such testing is not definitive.

"We think the risk to consumers at this point is remote," said Deborah Autor, director of FDA's drug compliance office, on a call with reporters.

The FDA report, which was posted online, lists more than 20 manufacturing problems found at the McNeil Consumer Healthcare plant in Fort Washington, Pa., where the formulas were made. The recalled products include children and infant formulations of Tylenol, Motrin, Zyrtec and Benadryl.

FDA inspectors visited the plant in mid-April and wrapped up their inspection Friday. J&J issued its "voluntary" recall later that night.

Among other problems, FDA inspectors said the company did not have laboratory facilities to test drug ingredients and failed to follow up on customer complaints.

J&J did not investigate more than 46 complaints received in the last year about "black or dark specks" in Tylenol products, according to the FDA's report.

Additionally, inspectors found some pieces of equipment covered with thick layers of dust, while others were held together with duct tape.

In a statement Tuesday, J&J called the problems cited by the FDA "unacceptable to us, and not indicative of how McNeil Consumer Healthcare intends to operate." The health conglomerate, which is based in New Brunswick, N.J., said production at the plant won't resume until the problems have been fixed.

The FDA reiterated that serious medical problems with the products are unlikely, but advised consumers to stop using the medicine as a precaution. Parents are instructed to use generic alternatives instead.

J&J's McNeil Consumer Healthcare unit has said some of the recalled medicines may have a higher concentration of the active ingredient than listed on the bottle. Others may contain particles, while still others may contain inactive ingredients that do not meet testing requirements.

FDA leadership told reporters Tuesday that they first met with J&J in February to discuss manufacturing problems identified in a warning letter about another J&J plant. The agency decided to step up inspections of the company's facilities based on those problems.

"That warning letter brought us to the point where we thought it was necessary to sit down with management and discuss our concerns," Autor said.

FDA officials said they are considering taking additional action against J&J, ranging from issuing more warning letters to pursuing criminal action.

Last week's sweeping recall, which involved products sold in the U.S. and 11 other countries, is the latest quality issue to taint J&J's over-the-counter medicine franchise. In January, the company recalled a line of adult Tylenol pain relievers due to complaints of a moldy smell associated with wooden pallets used to transport the drugs.
CAUTION: CHILDREN'S ZYRTEC - OR ANY OF THEIR SUGAR FREE PRODUCTS - CONTAINS SUCRALOSE (Splenda)

FDA Investigates Recall -WASHINGTON, Saturday May 1 – The Food and Drug Administration said Saturday it was investigating a health-care company for possible other problems following its recall of more than 40 over-the-counter infant's and children's liquid medications.

McNeil Consumer Healthcare Announces Voluntary Recall of Certain OTC Infants’ and Children's Products

Children's cold, allergy medicine recalled

Courtesy: Rense News Network

Tuesday, May 19, 2009

Why it pays to rely on nutritional supplementation

UPDATE: 11 June: BOO to BELO. BELO Broadcasting reports tonight on its KREM TV news outlet about Reglan yet makes no reference to safe B complex.
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One of the medical newsletters I receive arrived today with an article focused on the care of women who are pregnant.

The topic of the article was on treating a condition called hyperemesis gravidarum (HG) or severe nausea and vomiting during pregnancy.

The medical model of today is to offer drugs. The drugs offered in this report were metoclopramide (Reglan) plus diphenhydramine (Benadryl). Reglan has a caution for use during pregnancy. Benadryl contains aspartame which is not recommended for use in pregnancy.
May 18, 2009 — A protocol including metoclopramide plus diphenhydramine may be helpful for hyperemesis gravidarum (HG), the most severe form of nausea and vomiting during pregnancy, according to the results of a retrospective cohort study reported in the May issue of the European Journal of Obstetrics & Gynecology and Reproductive Biology.HG, the most severe form of nausea and vomiting of pregnancy, is intractable vomiting associated with weight loss of at least 5% of prepregnancy weight, dehydration, ketonuria, and hypokalemia. Second only to preterm labor, HG is a leading cause of hospitalization during pregnancy.

There is no gold standard for HG treatment, but droperidol (Inapsine Pregnancy: Category C: INAPSINE administered intravenously has been shown to cause a slight increase in mortality of the newborn rat at 4.4 times the upper human dose. At 44 times the upper human dose, mortality rate was comparable to that for control animals. Following intramuscular administration, increased mortality of the offspring at 1.8 times the upper human dose is attributed to CNS depression in the dams who neglected to remove placentae from their offspring. INAPSINE has not been shown to be teratogenic in animals. There are no adequate and well-controlled studies in pregnant women. INAPSINE should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.) and diphenhydramine have been used since 1998. Warnings about the cardiovascular toxicity of injectable droperidol, including QT prolongations, serious arrhythmia, and sudden death, were issued by the US Food and Drug Administration in December 2001 and subsequently by Health Canada. A new HG protocol replacing droperidol with metoclopramide has been used since June 2002 but has not previously been evaluated.
Eur J Obstet Gynecol Reprod Biol. 2009:143:43-49.

Depletion of B complex vitamins in pregnancy is related to nausea and vomiting as well as HG based on nutritional research.

The use of B vitamins will resolve this issue and they do not cause risk to the fetus or the mother's health.

Our nutritional powder, RK BioBlend, has helped many people over the years with this health concern in a safe and effective manner. The B vitamins also help prevent birth defects related to many issues especially neural tube defects (Spina Bifida).

Perhaps you'd like your toast and butter spread with nutritional yeast?

 
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