Prescription Drug Recalls & Safety News


Over The Counter Cough and Cold Medications
Thu, 09 Oct 2008 16:40:00 EDT

Product labels being modified to state "do not use" in children under 4 years of age.



Tiotropium (marketed as Spiriva HandiHaler)
Tue, 07 Oct 2008 11:32:00 EDT

UPDATE - Preliminary results of the UPLIFT Trial shows no increased risk of stroke with tiotropium bromide. Two recent publications reported increased risk for mortality and/or cardiovascular events in patients who received tiotropium or inhaled anticholinergics.

Nebion HLX-8 Magnetic Resonance Device
Fri, 03 Oct 2008 16:10:00 EDT

Device recalled because it was not approved by FDA, lacked safety and effectiveness data, and was not manufactured under current good manufacturing practices.

Medtronic Neuromodulation INDURA One-Piece Intrathecal Catheters, Sutureless Pump Connector Revision Kit, Intrathecal Catheter Pump Segment Revision Kit
Thu, 02 Oct 2008 10:50:00 EDT

Class I Recall because of potential misconnections of the Medtronic sutureless connector catheters from the catheter port on the pump.

October 2008 Patient Safety News
Wed, 01 Oct 2008 17:55:00 EDT

Patient Safety News is a video news show for healthcare professionals, covering safety alerts, recalls, product approvals, and important tips on protecting patients.

Statin drugs and amyotrophic lateral sclerosis (ALS)
Tue, 30 Sep 2008 11:00:00 EDT

New analysis of 41 long-term controlled clinical trials provides evidence that use of statins does not increase incidence of ALS.

Epoetin alfa
Fri, 26 Sep 2008 11:10:00 EDT

Preliminary safety findings from a German clinical trial showed more deaths in patients given epoetin-alpha versus placebo.

Ammonul (sodium phenylacetate and sodium benzoate) Injection 10%/10%
Tue, 23 Sep 2008 14:35:00 EDT

Particulate matter detected in product. Healthcare providers instructed to use a filter during the admixture process.

Tarceva (erlotinib)
Tue, 23 Sep 2008 14:35:00 EDT

Cases of hepatic failure and hepatorenal syndrome, including fatalities, have been reported during use of Tarceva, particularly in patients with baseline hepatic impairment.

Infant Formula Manufactured in China Contaminated With Melamine
Mon, 22 Sep 2008 11:25:00 EDT

UPDATE - FDA investigation of Asian markets found no Chinese-manufactured infant formula on shelves.

If you or a loved one suffered serious injury while taking a pharmaceutical product, you may wish to contact a qualified attorney who can evaluate your case to determine the best way to protect your legal rights. You may be entitled to compensation for your losses and suffering. Please contact our office to speak to an attorney today for a free consultation.
 

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