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Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure

Teva Pharmaceuticals USA has initiated a voluntary nationwide recall of a single lot of Anagrelide Capsules, USP 0.5 mg (Lot number GD01090), to the consumer level in the United States. This voluntary recall was initiated due to dissolution test failure detected during routine stability testing. No

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/teva-issues-voluntary-nationwide-recall-one-lot-anagrelide-capsules-usp-05-mg-due-dissolution-test

 
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The #COVID19 🦠 vaccine is safe and recommended 👍🏽 for women anyone planning a pregnancy 🤰🏻. 🧑🏾‍⚕️ Talk to your

The #COVID19 🦠 vaccine is safe and recommended 👍🏽 for women anyone planning a pregnancy 🤰🏻.

🧑🏾‍⚕️ Talk to your healthcare provider to make an informed decision about vaccination.

#GetVax as soon as it is your turn 🩹❤️
➡️ paho.org/en/covid-19-va… https://t.co/uAfPPEPZxI