Does HUMIRA Cause Incorrect product storage? 149 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 149 reports of Incorrect product storage have been filed in association with HUMIRA. This represents 0.4% of all adverse event reports for HUMIRA.
149
Reports of Incorrect product storage with HUMIRA
0.4%
of all HUMIRA reports
0
Deaths
4
Hospitalizations
How Dangerous Is Incorrect product storage From HUMIRA?
Of the 149 reports, 4 (2.7%) required hospitalization.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for HUMIRA. However, 149 reports have been filed with the FAERS database.
What Other Side Effects Does HUMIRA Cause?
Injection site pain (6,005)
Drug ineffective (3,506)
Arthralgia (2,204)
Pain (2,045)
Fatigue (1,868)
Psoriasis (1,857)
Injection site erythema (1,654)
Injection site bruising (1,623)
Headache (1,582)
Nasopharyngitis (1,552)
What Other Drugs Cause Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which HUMIRA Alternatives Have Lower Incorrect product storage Risk?
HUMIRA vs HUMIRA PEN
HUMIRA vs HYALURONATE
HUMIRA vs HYALURONIC ACID
HUMIRA vs HYALURONIC ACID\LIDOCAINE
HUMIRA vs HYALURONIDASE