IBANDRONATE SODIUM
Generic: IBANDRONATE SODIUM
Aurobindo Pharma LimitedManufacturer
ORALRoute
IBANDRONATE SODIUMActive Substance
2016-03-11Original Approval
IBANDRONATE SODIUM is FDA application ANDA204502, sponsored by AUROBINDO PHARMA. 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
ARTHRALGIA
261 reports
2
DIARRHOEA
244 reports
3
NAUSEA
238 reports
4
FEMUR FRACTURE
219 reports
5
HEADACHE
217 reports
6
FATIGUE
212 reports
7
DIZZINESS
178 reports
8
FALL
176 reports
9
PAIN
167 reports
10
ASTHENIA
160 reports