CIMETIDINE
Generic: CIMETIDINE
Aurobindo Pharma LimitedManufacturer
ORALRoute
CIMETIDINEActive Substance
2024-11-12Original Approval
CIMETIDINE is FDA application ANDA218997, sponsored by AUROBINDO PHARMA LTD. 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.
Top Reported Reactions
1
CHRONIC KIDNEY DISEASE
892 reports
2
ACUTE KIDNEY INJURY
501 reports
3
RENAL FAILURE
433 reports
4
NAUSEA
423 reports
5
FATIGUE
394 reports
6
DRUG INEFFECTIVE
335 reports
7
DYSPNOEA
297 reports
8
VOMITING
290 reports
9
DIARRHOEA
259 reports
10
DIZZINESS
231 reports