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FeaturedIn a recent update, the Medicines and Healthcare products Regulatory Agency (MHRA) has released important information regarding statins and their potential link to myasthenia gravis. This announcement comes…
FeaturedThe Pharmacovigilance Risk Assessment Committee (PRAC) convened from September 25th to 28th, 2023, to review critical safety data. Among the significant outcomes was the decision to update the…
FeaturedThe U.S. Food and Drug Administration (FDA) has taken a monumental step towards combating rare diseases. In a recent announcement, the agency disclosed the allocation of $27 million…
Introducing the Vaccine Monitoring Platform (VMP) research agenda The European Medicines Agency (EMA) and the European Centre for Disease Prevention and Control (ECDC) have introduced the Vaccine Monitoring…
In a recent development, the European Medicines Agency’s (EMA) human medicines committee (CHMP) has recommended against renewing the conditional marketing authorization for Blenrep (belantamab mafodotin), a medicine primarily…
ImportantDear Healthcare Providers, We are writing to inform you of an important safety notice regarding Terumo Platelet Additive Solution+ (T-PAS+). Please carefully review the following information: Device Details:…
FeaturedIn a critical advisory, healthcare professionals are being urged to exercise utmost caution when prescribing fluoroquinolone antibiotics (ciprofloxacin, delafloxacin, levofloxacin, moxifloxacin, ofloxacin). This class of antibiotics, while effective,…
FeaturedWe want to bring to your attention an urgent recall affecting two specific batches of Lipocomb capsules, Lipocomb 10 mg/10 mg (batch PPA0465/460/001) and Lipocomb 20 mg/10 mg…
: In a move to ensure the safety and efficacy of weight management medications, the European Medicines Agency (EMA) has recently launched a comprehensive review of Mysimba (naltrexone/bupropion).…
Advancements in Device Safety Communication: The FDA’s Center for Devices and Radiological Health (CDRH) has released a comprehensive report to Congress on Postmarket Device Safety-Related Communications. This initiative…
ImportantWe would like to bring to your attention an important recall notice regarding Ketofall 0.25 mg/ml Eye Drops Solution in single-dose containers. Background Information: The Health Products Regulatory…
We would like to bring to your attention an important recall notice regarding certain products manufactured by Sun Pharma UK Ltd. Specifically, this alert pertains to Gemcitabine 10mg/ml…
In a progressive move towards safeguarding the public’s health and interests, the UK government has officially commenced a consultation on unregulated cosmetic procedures. This significant step is aimed…
The European Medicines Agency (EMA) is taking proactive steps to safeguard the health of expectant mothers and their unborn children by recommending new measures to avoid exposure to…
FeaturedThe Department of Health – Abu Dhabi (DoH) has closed a medical laboratory in the Emirate for violating regulations. The laboratory, which is located in Al Ain, was…
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