Does ABATACEPT SUBQ /ML Cause Incorrect product storage? 45 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Incorrect product storage have been filed in association with ABATACEPT SUBQ /ML. This represents 3.9% of all adverse event reports for ABATACEPT SUBQ /ML.
45
Reports of Incorrect product storage with ABATACEPT SUBQ /ML
3.9%
of all ABATACEPT SUBQ /ML reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product storage From ABATACEPT SUBQ /ML?
Of the 45 reports, 1 (2.2%) 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 ABATACEPT SUBQ /ML. However, 45 reports have been filed with the FAERS database.
What Other Side Effects Does ABATACEPT SUBQ /ML Cause?
Drug ineffective (216)
Drug dose omission (88)
Pain (55)
Nasopharyngitis (48)
Fatigue (42)
Headache (41)
Nausea (36)
Sinusitis (36)
Malaise (34)
Product quality issue (33)
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 ABATACEPT SUBQ /ML Alternatives Have Lower Incorrect product storage Risk?
ABATACEPT SUBQ /ML vs ABEMACICLIB
ABATACEPT SUBQ /ML vs ABIRATERONE
ABATACEPT SUBQ /ML vs ABOBOTULINUMTOXINA
ABATACEPT SUBQ /ML vs ABROCITINIB
ABATACEPT SUBQ /ML vs ACALABRUTINIB