Safety Alerts & Recalls

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Latest Alerts

Puren Pharma ruft alle Chargen von Moxonidin-Actavis 0,3 mg und 0,4 mg Filmtabletten zurück
Die Firma Puren Pharma GmbH & Co. KG ruft alle Chargen Moxonidin-Actavis 0,3 mg und Moxonidin-Actavis 0,4 mg Filmtabletten, jeweils Packungen mit 100 Stück, vom Markt zurück. Die Medikamente werden zurückgerufen, weil die Zulassung für diese Medikamente am 01 Januar 2018 erloschen ist und sie nach diesem Datum nicht mehr verkauft werden dürfen. Moxonidin-Actavis 0,3 mg und Moxonidin-Actavis 0,4 mg Filmtabletten werden zur Behandlung von hohem Blutdruck (Hypertonie) eingesetzt. Dieser Rückruf betrifft nur Moxonidin-Actavis 0,3 mg und Moxonidin-Actavis 0,4 mg Filmtabletten. Keine anderen Stärken und keine Moxonidin-Präparate anderer Hersteller sind von dem Rückruf betroffen. Weitere Informationen finden Sie unter: http://www.drugbase.de/de/datenbanken/abda-datenbank/aktuelle-infos/artikel.html?tx_ttnews%5Btt_news%5D=2178002&tx_ttnews%5BbackPid%5D=115&cHash=a8e4f4b46a26226747cd17b58926cdb1
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Teva Pharmaceuticals USA Recalls Single Lot of Nabumetone 750 mg Tablets
Teva Pharmaceuticals USA has recalled a single lot of Nabumetone 750 mg tablets. Lot number 05N533 is being recalled because there were missing labels and leaflets. Nabumetone is often used in the treatment of pain. This recall alert only applies to the single lot of the generic Nabumetone Tablets, 750 mg made by Teva Pharmaceuticals USA. No other nabumetone products were involved in this recall. To search for an view the FDA notice about this recall, please visit: http://www.accessdata.fda.gov/scripts/ires/index.cfm
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Date Published Title Medicine Source
2018-01-02 Puren Pharma ruft alle Chargen von Moxonidin-Actavis 0,3 mg und 0,4 mg Filmtabletten zurück Moxonidine AMK
2016-07-06 Teva Pharmaceuticals USA Recalls Single Lot of Nabumetone 750 mg Tablets Nabumetone FDA
2016-02-03 Los Profesionales Sanitarios Informados: Viekirax (Ombitasvir, Paritaprevir, Ritonavir) No Recomendado En Pacientes Con Determinados Problemas En El Hígado AEMPS
2015-02-25 Product Information Updated after Warfarin Review Warfarin TGA
2015-02-20 Counterfeit Cialis Warning Tadalafil TGA
2015-02-20 Metoclopramide Associated with Neurological Effects Metoclopramide TGA
2015-02-20 Combined Oral Contraceptive Implicated in Inflammatory Bowel Disease Desogestrel with Ethinylestradiol TGA
2015-02-13 Recall of Three Batches of Akineton 2mg Tablets from Link Healthcare Biperiden TGA
2014-12-08 Mucokehl 'i' Solution Poses Infection Risk TGA
2014-12-08 Panadol 1-5 Years Colourfree Suspension May Cause Confusion about Dosing Panadol Extra TGA
2014-12-08 Zovirax Eye Ointment Recall Aciclovir TGA
2014-06-19 Strontium Risks Highlighted in New Safety Warning TGA
2014-06-19 Risk of High Fevers with Meningococcal Vaccine TGA
2014-05-14 Alere Recalls Alere INRatio2 PT/INR test strips Warfarin TGA
2014-05-14 Accu-Check Mobile Recall due to antibiotic interference Ceftriaxone TGA
2014-05-14 Codeine in Children - US Deaths Spark New Safety Warnings TGA
2014-05-14 Sprue-Like Enteropathy Risk with Olmesartan Usage TGA
2014-05-14 Emergency Contraceptive Effectiveness Questioned Levonorgestrel TGA
2014-05-14 Recall of FreeStyle Lite Blood Glucose Strips Insulin Aspart TGA
2014-04-29 Xyntha Recalled Because of Incorrect Labelling Refacto TGA