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Baxter Healthcare Corporation have informed the MHRA that the Patient Information Leaflet (PIL) packed in specified batches does not contain up to date information relating to the duration of contraception required for females after stopping taking this medication.
Change to the information provided in the Summary of Product Characteristics for Bioestrovet Swine 0.0875 mg/ml Solution for Injection for Pigs.
This guide is about infections that occur in people who inject drugs (PWID).
Actions following the identification of the cause of an increase of adverse event reports following the use of Genta-Equine 100 mg/ml Solution for Injection for Horses.
Viatris has received reports of brown discolouration and blockage in the needle of pre-filled syringes of Arixtra. This quality defect is related to oxidation of the syringe needle.
Change to the information provided on adverse events in the Summary of Product Characteristics (SPC).
Bio Products Laboratory Limited is recalling one batch of Human Rabies Immunoglobulin following a stability failure for this batch. The batch has shown a reduction in potency of the Human Rabies immunoglobulin.
Results of in-depth assessment of reports of death, arthritis and human exposure following administration of Librela in dogs in the United Kingdom.
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