Does HYDROXYCHLOROQUINE Cause Product dose omission? 114 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 114 reports of Product dose omission have been filed in association with HYDROXYCHLOROQUINE (HYDROXYCHLOROQUINE SULFATE). This represents 0.2% of all adverse event reports for HYDROXYCHLOROQUINE.
114
Reports of Product dose omission with HYDROXYCHLOROQUINE
0.2%
of all HYDROXYCHLOROQUINE reports
1
Deaths
8
Hospitalizations
How Dangerous Is Product dose omission From HYDROXYCHLOROQUINE?
Of the 114 reports, 1 (0.9%) resulted in death, 8 (7.0%) required hospitalization, and 1 (0.9%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROXYCHLOROQUINE. However, 114 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROXYCHLOROQUINE Cause?
Drug ineffective (31,057)
Rheumatoid arthritis (20,110)
Off label use (15,318)
Drug intolerance (14,093)
Pain (13,524)
Joint swelling (11,353)
Fatigue (11,342)
Contraindicated product administered (10,557)
Arthralgia (10,367)
Abdominal discomfort (9,910)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which HYDROXYCHLOROQUINE Alternatives Have Lower Product dose omission Risk?
HYDROXYCHLOROQUINE vs HYDROXYCHLOROQUINE DIPHOSPHATE
HYDROXYCHLOROQUINE vs HYDROXYETHYL STARCH 130/0.4
HYDROXYCHLOROQUINE vs HYDROXYPROGESTERONE
HYDROXYCHLOROQUINE vs HYDROXYPROGESTERONE CAPROATE
HYDROXYCHLOROQUINE vs HYDROXYPROPYL CELLULOSE