Tag: Drug side effects

Lawsuit Blames Chicago Woman’s Death on Botox

Botox™, made of botulinum toxin, one of the most potent poisons in the world. Incorrect injection can cause death from symptoms of botulism.

A woman injected with cosmetic Botox at a skin care center in Chicago in May, 2011 developed symptoms of botulism and died, and her husband is suing the doctor who injected her.

In May, 2011, after receiving injections of Botox, Janet Rosenstern, 55, started suffering progressive generalized muscle weakness. She eventually became unable to hold up her neck. She developed weakness in muscles throughout her body, developed severe anxiety, truncal parasthesias (feelings of prickling, burning or tingling in the skin) dizziness, unsteady gait, muscle spasms and involuntary jerking-type movements in her abdominal wall.

She contacted her doctor immediately after her Botox injections and reported her symptoms, but the doctor was dismissive of her complaints. She went to the emergency room several times as her symptoms worsened.

After suffering with these progressively worsening symptoms for nearly a year, on April 22, 2012, she was found unconscious and died the next day.

Her husband, Klaus Rosenstern, is suing his wife’s doctor, Steven Dayan of the True Skin Care Center in Chicago, seeking damages for negligence, lack of informed consent, medical battery and wrongful death. He charges that Dr. Dayan failed to inform his wife of the known serious, debilitating and deadly potential side effects of being injected with Botox Cosmetic.

Botox is Allergan’s trade name for botulinum toxin, one of the most potent neurotoxins in the world. If it spreads through the body, it can cause death.

Janet Rosenstern was a registered nurse who is described in the lawsuit as a “high functioning” and “articulate” woman.

People who have had serious reactions from injections of Botox, like a woman in British Columbia who ended up paralyzed and in a wheelchair, are struggling to make others aware of the serious risks of being injected with Botox.

Source: Courthouse News Service, Tuesday, April 29, 2014

FDA Orders Sexual Dysfunction Warning Added for Merck Baldness Drug Propecia

If your hairline is receding and you’re are thinking about taking Merck’s baldness drug Propecia, you might want to think again. The U.S. Food and Drug Administration (FDA) ordered drug maker Merck to change the warning labels for Propecia and its prostate drug Proscar to include “libido disorders, ejaculation disorders and orgasm disorders,” conditions that FDA notes may continue well after patients stop taking the drugs.  While FDA says it isn’t clear whether finasteride, the active chemical in Propecia and Proscar, is what causes the persistent sexual problems, side effects reported by those using the drugs “suggest a broader range of adverse effects than previously reported in patients taking these drugs.” FDA approved Proscar in 1992 and Propecia in 1997.  Since then, the agency has reviewed 421 post-marketing reports of sexual dysfunction from those taking Propecia between 1998 and 2011. Of those, 59 cases described sexual dysfunction lasting a minimum of three months after discontinuing Propecia. FDA reviewed 131 reports of similar problems associated with Proscar. In 2011, FDA ordered the warning labels of both product be revised to include erectile dysfunction that continues after patients stop taking the drug.  People can report adverse side effects of prescription drugs to FDA’s MedWatch hotline at 1-800-332-1088, report them online at MedWatch Online or through the U.S. mail using the MedWatch form (pdf) available at FDA’s website.

Source: U.S. Food and Drug Administration, April 11, 2012