Since Actemra (tocilizumab) hit the market in 2010, the U.S. Food and Drug Administration (FDA) has received at least 13,500 adverse event reports link to the drug, including 1,128 reports of death, according to a recent investigation by STAT. Actemra was approved to treat rheumatoid arthritis (RA) in 2010. In May 2017, the FDA approved Actemra for treatment of another auto-immune disease called giant cell arteritis.
Actemra Dangers
Some of the potential side effects listed on the Actemra label include:
- Cancer
- Severe allergic reaction
- Nervous system problems
- Gastrointestinal tears
- Serious infections, including hepatitis B
Potential side effects that are not included in the warning label include:
- Pancreatitis
- Lung complications, including interstitial lung disease
- Heart attack
- Heart failure
- Stroke
Failure to Warn
If you have been harmed by Actemra or lost a loved one to Actemra side effects, you may be able to recover substantial compensation. Drug makers have a duty to warn consumers, doctors and other health care professionals about the dangers associated with their products. This gives doctors the opportunity to give their patients informed guidance and gives patients the chance to make an informed choice.
According to the STAT report, other RA drugs that carry the same risk of life-threatening side effects, or possibly lower, do carry warnings while Actemra does not, leading patients to believe that Actemra is a safer choice. STAT’s review of the adverse event reports shows that Actemra is not safer.
If you have been harmed by Actemra, please talk to an experienced Actemra injury attorney right away to learn more about your rights and potential compensation.
Didn’t we go through this before with BEXTRA? I take up to 20-40mg LORTAB 10/325mgs a day when it is raining or if I worked out heavily for my Industrial Accident (Comminuted Facture, Tib/Fib Distal third LT Leg) and as one knows Opioids cause all kinds of problems beyond addiction/overdose. NSAIDS just chew up my insides (Bloody Stools) and they simply do not have the pain quelling properties that Lortab have. My doctor had prescribed BEXTRA and had given me about 100 free samples when he phoned me at home and told me not to take it (SEVERE ADVERSE REACTIONS led to market withdraw).
I know of three drugs that my physician is following, two of which I have taken.. Cipro (Antibotic), Methadone (which I won’t take…I casual friend of mine lost her son because he took O-N-E Methadone pill for his football injuries (because the line between efficacy & Overdose are soooo small…) and A-N-Y kind of NSAIDS (GI track issues). If there has been a minimum 1,300 deaths from ACTEMRA, that stuff needs to be yanked from the market!!!