August 7, 2019 at 10:42 am

FDA States Novartis May Face Criminal Charges

Novartis pharmaceuticals knowingly used inaccurate data when applying for FDA approval of its $2.1 million gene therapy drug,” states FDA. The drug is the most expensive drug in the world, costing users $2.1 million per one-time use.
Criminal actions against the company may be taken. Read the full article here.
August 6, 2019 at 5:48 pm

Young Girl Developed Suicidality After Prescriptions

Researching the cocktails of drugs doctors prescribed to her young child, Ms. Parker discovered that one of the drugs was used as a sedative for violent inmates in Canadian prisons.
“I thought, if that’s being given to grown men in prison in Canada, why are you giving it to my child?”
Read the full article here.
August 3, 2019 at 8:33 am

Teen’s Hallucinations & Death May Be Linked to Adverse Drug Effects

Mefloquine, an anti-malaria drug known to cause severe adverse effects including hallucinations, insomnia, panic attacks, nightmares and suicide, may have precipitated a young British teen’s sudden death.
Guidance from the National Institute of Health and Care Excellence (Nice) says: “Mefloquine is associated with potentially serious neuropsychiatric reactions.
Read the full article here.
August 1, 2019 at 4:38 pm

Drug Labels Need Attention

“Labeling can be confusing, vague, misleading, hidden in medical jargon or missing altogether,” said Rachel Brummert, a patient advocate and FDA special employee. “If prescription labeling were consistent, we could avoid many of the problems caused by inconsistent labeling.”
Read the full article here.

 

July 26, 2019 at 1:44 pm

Drug Risks Should be Clearly Communicated

Prescription drug withdrawal can sometimes lead to permanent prescriptions. “Ten years on and I am still taking that antipsychotic, not because it proved to be an effective mood stabilizer, not because it improves my health in any way, but simply because I am physically incapable of sleep without it.”
Read the full article here.
July 25, 2019 at 2:28 pm

Drug Safety Label Changes: A Target for Collaboration
“Communicating the most up-to-date information on a product’s safety to patients and providers is one of FDA’s most important functions,” said Mark McClellan, MD, PhD, director of Duke Margolis Center for Health Policy.
Collaboration is needed to help the FDA increase its understanding of the impact of postmarketing drug safety. Read the full press release here.
July 22, 2019 at 5:21 pm

A Solution to Increasingly High Drug Prices?

High drug costs can lead to people skipping their prescriptions. This can lead to many serious adverse drug effects to include withdrawal akathisia. Read the full article here.
July 20, 2019 at 1:30 pm

HIV Patients File New Lawsuit Over Adverse Drug Effects

Two new lawsuits charge many patients taking a Gilead HIV drug “needlessly suffered debilitating and sometimes fatal kidney and bone damage as well as damage to their teeth.” Read the full article here.
July 20, 2019 at 10:48 am

11.9K New Views to MISSD YouTube Channel

MISSD can’t help but be thrilled with these new analytics: More than 11.9K new views to our YouTube Channel in less than 90 days. Viewers from across the globe include India, USA, Saudi Arabia, Canada…
We are grateful to all who help us increase awareness of adverse drug effects.
July 19, 2019 at 1:37 pm

Drug Risks Often Identified After FDA Approval

Sixty two percent of this specific drug class received the FDA’s most stringent warning, known as a “black box.” Most of the serious adverse effects were identified only after the drugs were on the market.
 “It raises the question of should we be regulating them differently,” said Joseph Ross, an associate professor of medicine at Yale School of Medicine, who has studied drug safety. Read the full article here.