In that case, the licence holder should submit a follow-up report citing the original adverse reaction ... health products that were used at the same time as the adverse reaction describe if any drugs ...

This allowed for the continued use of almonertinib without any adverse reactions. Based on these observations, we lean towards considering cutaneous vasculitis caused by EGFR-TKIs is a drug-induced ..

Reported adverse effects include gastrointestinal, pulmonary, hepatic and neurological disorders. We report a case ... that the adverse drug reaction is due to the drug itself.11 According to the ...

Neuroleptic malignant syndrome (NMS) is a potentially lethal adverse drug reaction. We report a case of NMS potentially induced by dehydration in a female patient suffering from schizoaffective ...

Adverse drug reactions (ADRs) remain a common clinical problem since they can mimic many diseases and cause significant morbidity and mortality. Judicious prescribing is important to minimize ...

John Larson abruptly stopped talking while he was on the floor of the House of Representatives in Washington, D.C., with his office reportedly saying he had an "adverse reaction" to new medication.

This afternoon, he had what was likely an adverse reaction to a new medication and ... according to a report from the Pew Research Center. In January, Pew reported that the average age of voting ...

John Larson stalled and seemingly froze mid-speech on the House of Representatives floor, according to an alarming clip of the moment — which his team claimed was an “adverse reaction” to a ...

The U.S. Food and Drug Administration is raising alarms about Librela, warning veterinarians of potential adverse effects, including death, in some dogs receiving the treatment.

The U.S. Food and Drug Administration announced last week that a pharmaceutical company is removing a fentanyl patch from ...

However, in its fourth-quarter earnings release this morning, the biopharma announced that the trial has been placed on hold by the FDA “following a single adverse event report of a case of ...