ATENOLOL
Generic: ATENOLOL
Mylan Pharmaceuticals Inc.Manufacturer
ORALRoute
ATENOLOLActive Substance
1992-01-24Original Approval
ATENOLOL is FDA application ANDA073457, sponsored by MYLAN. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Recalls
Class II2017-03-06
ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-0Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP
Class II2014-08-05
ZyGenerics ATENOLOL Tablets, USP 25 mg 1000 count bottle, Rx Only Manufactured by: Cadila Healthcare Ltd. Ahmedabad, IndSuperpotent Drug: A complaint was reported by a pharmacist who stated several tablets were noticeab
Top Reported Reactions
1
DRUG INEFFECTIVE
7,567 reports
2
NAUSEA
7,423 reports
3
FATIGUE
7,187 reports
4
DIARRHOEA
6,657 reports
5
DYSPNOEA
5,910 reports
6
DIZZINESS
5,891 reports
7
HEADACHE
5,601 reports
8
PAIN
5,431 reports
9
ASTHENIA
4,656 reports
10
FALL
4,381 reports