Does CROTALIDAE POLYVALENT IMMUNE FAB Cause Condition aggravated? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Condition aggravated have been filed in association with CROTALIDAE POLYVALENT IMMUNE FAB. This represents 2.1% of all adverse event reports for CROTALIDAE POLYVALENT IMMUNE FAB.
14
Reports of Condition aggravated with CROTALIDAE POLYVALENT IMMUNE FAB
2.1%
of all CROTALIDAE POLYVALENT IMMUNE FAB reports
0
Deaths
6
Hospitalizations
How Dangerous Is Condition aggravated From CROTALIDAE POLYVALENT IMMUNE FAB?
Of the 14 reports, 6 (42.9%) required hospitalization.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CROTALIDAE POLYVALENT IMMUNE FAB. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does CROTALIDAE POLYVALENT IMMUNE FAB Cause?
Pain (68)
Swelling (67)
Peripheral swelling (61)
Off label use (57)
Underdose (57)
Thrombocytopenia (52)
Rash (51)
Anaphylactic reaction (45)
Inappropriate schedule of product administration (45)
Platelet count decreased (45)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which CROTALIDAE POLYVALENT IMMUNE FAB Alternatives Have Lower Condition aggravated Risk?
CROTALIDAE POLYVALENT IMMUNE FAB vs CUBICIN
CROTALIDAE POLYVALENT IMMUNE FAB vs CUPRIC
CROTALIDAE POLYVALENT IMMUNE FAB vs CUPRIC ANHYDROUS
CROTALIDAE POLYVALENT IMMUNE FAB vs CUPRIC\FOLIC ACID\NIACIN\ZINC
CROTALIDAE POLYVALENT IMMUNE FAB vs CX-024414