HYDROXYCHLOROQUINE SULFATE
Generic: HYDROXYCHLOROQUINE SULFATE
Aurobindo Pharma LimitedManufacturer
ORALRoute
HYDROXYCHLOROQUINE SULFATEActive Substance
1998-05-29Original Approval
HYDROXYCHLOROQUINE SULFATE is FDA application ANDA040274, sponsored by AUROBINDO PHARMA USA. 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
18,226 reports
2
RHEUMATOID ARTHRITIS
13,803 reports
3
PAIN
10,908 reports
4
FATIGUE
9,495 reports
5
DRUG INTOLERANCE
9,339 reports
6
OFF LABEL USE
8,570 reports
7
ARTHRALGIA
8,482 reports
8
JOINT SWELLING
8,477 reports
9
CONTRAINDICATED PRODUCT ADMINISTERED
8,143 reports
10
ALOPECIA
7,794 reports