Does HYDROXOCOBALAMIN Cause Product use issue? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product use issue have been filed in association with HYDROXOCOBALAMIN (Cyanokit). This represents 2.8% of all adverse event reports for HYDROXOCOBALAMIN.
14
Reports of Product use issue with HYDROXOCOBALAMIN
2.8%
of all HYDROXOCOBALAMIN reports
4
Deaths
2
Hospitalizations
How Dangerous Is Product use issue From HYDROXOCOBALAMIN?
Of the 14 reports, 4 (28.6%) resulted in death, 2 (14.3%) required hospitalization.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HYDROXOCOBALAMIN. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does HYDROXOCOBALAMIN Cause?
Acute kidney injury (64)
Somnolence (62)
Coma (59)
Product use in unapproved indication (57)
Gastrooesophageal reflux disease (50)
Pneumonia aspiration (50)
Chromaturia (48)
Off label use (42)
Drug ineffective (41)
Underdose (26)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which HYDROXOCOBALAMIN Alternatives Have Lower Product use issue Risk?
HYDROXOCOBALAMIN vs HYDROXYCHLOROQUINE
HYDROXOCOBALAMIN vs HYDROXYCHLOROQUINE DIPHOSPHATE
HYDROXOCOBALAMIN vs HYDROXYETHYL STARCH 130/0.4
HYDROXOCOBALAMIN vs HYDROXYPROGESTERONE
HYDROXOCOBALAMIN vs HYDROXYPROGESTERONE CAPROATE