ERGOCALCIFEROL
Generic: ERGOCALCIFEROL
Bionpharma Inc.Manufacturer
ORALRoute
ERGOCALCIFEROLActive Substance
1978-10-16Original Approval
ERGOCALCIFEROL is FDA application ANDA080704, sponsored by BIONPHARMA. 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
DRUG INEFFECTIVE
4,644 reports
2
FATIGUE
4,377 reports
3
PAIN
4,279 reports
4
OFF LABEL USE
4,182 reports
5
DYSPNOEA
4,097 reports
6
HEADACHE
3,744 reports
7
NAUSEA
3,744 reports
8
DIARRHOEA
3,527 reports
9
VOMITING
3,458 reports
10
ARTHRALGIA
3,385 reports