Articles Posted in Defective Drugs

Excelsior Disposable 5mL fill in 6mL prefilled saline flush syringes are supposed to be used for the flushing of venous access devices, such as inserted central catheters and intravenous (IV) lines. However, a batch of these syringes that were distributed in August 2010 has now been determined to create risks for those who require the…

There’s another Tylenol recall. This time it is the company’s 8 Hour Caplets 50 Count, lot number BCM155. McNeil is recalling TYLENOL 8 Hour caplets 50 count bottles from retail shelves following a number of complaints about an odor being emitted from the bottles. This unhealthy odor is a moldy, musty smell that has been…

The Meredia Diet Pill has recently been recalled by the Federal Drug Administration. On October 8, 2010, this drug was removed from the United States Market, including Illinois and Indiana. Previously, the Meredia Diet Pill had been banned from Europe and Australia. The drug is manufactured by Abbot Drugs, located in Lake County, Illinois. The…

Nearly two years ago, the FDA received a high number of adverse events reports relating to Gadolinium-based (GADO) Contrast Dyes used in MRI testing. Adverse events reports are used to describe incidents in which a user of a drug is injured because of the ingredients in the product. In the case of GADO dye, a…

In Indiana, laws already restrict the sale of methamphetamine and related over-the-counter drugs such as select cold medicines which contain meth. Today, Indiana lawmakers are taking meth restrictions to the next level with the introduction of a proposal that would not allow pharmacies to sell pseudoephedrine without a prescription from a physician. Indiana lawmakers believe…

Sixty two dietary supplement products have been removed from the nationwide and international market following an investigation uncovering that the supplements contain steroid or steroid-like substances that were not approved by the FDA. The recalling firm is Bodybuilding.Com, Meridian, ID. The recall began in November 2009 and is still ongoing, including: D-DROL capsules, D-Drol Complex…

If you’ve been using Qualaquin (quinine sulfate) to prevent leg cramps, treat leg cramps or for restless leg syndrome, you need to know that two people using Qualaquin and 36 others have experienced serious life threatening side effects between April and October 2008. This link was discovered after the FDA reviewed its Adverse Event Reporting…

Reglan, manufactured by Baxter Healthcare Corporation, has long been used in over 2 million children and adults for the treatment of gastrointestinal conditions such as diabetic gastroparesis disease and gastroesophageal reflux disease. The ill effects of Reglan use has not become fully apparent until recently. The FDA has announced that long term and high dose…

In November of 2009, Yaz and a similar product Ocella were recalled following reports of serious injury in users as young as thirteen years old. The problems associated with Yaz and Ocella involve the dosage of drospirenone which is known for creating health problems in users that live in European countries. In fact, the use…

Prempro is subject to another cause for alarm because of a recent recall. This drug recall affects two lots of the product, namely Lot C83323 (exp. 3-10) and Lot D82196 (exp. 12-10). Nearly, 50,000 cartons of Prempro are included in this particular drug recall. Wyeth Pharmaceuticals, the manufacturer of Prempro, began the drug recall in…