Many medications cause known side effects. Typically, however, a doctor prescribing a drug will determine the benefits outweigh the dangers of taking them. Doctors cannot make this determination for their patients, though, and therefore they have an obligation to advise them of the risks of harm associated with the treatment they recommend. If they do not, they may be held responsible for losses their patients subsequently suffer, even if they arise out of established risks. Lack of informed consent claims must be filed in a timely manner; however, otherwise, they may be time-barred, as demonstrated in a recent ruling issued by a Maryland court. If you sustained injuries due to your doctor’s failure to advise of the risks associated with a treatment, you should meet with a knowledgeable Maryland medical malpractice lawyer to discuss what claims you may be able to pursue.
The Plaintiff’s Harm
It is reported that in 2010, the plaintiff was treated by the defendant pulmonologist due to complaints of shortness of breath and a chronic cough. The defendant diagnosed the plaintiff with numerous lung conditions and initial treated him with a steroid. When the plaintiff did not improve, the defendant doctor prescribed Cytoxan. He slowly began to improve and continued to take the medication until May 2013.
Allegedly, the plaintiff married in 2016. After trying to conceive for a year with no success, he visited a fertility specialist, who determined he had no viable sperm. The specialist attributed this to Cytoxan toxicity. The plaintiff then filed a lack of informed consent claim against the defendant. The defendant moved for dismissal, arguing the plaintiff’s claims were barred by the statute of limitations. Continue Reading ›
Published by Arfaa Law Group












