Does ABATACEPT SUBQ /ML Cause Product quality issue? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Product quality issue have been filed in association with ABATACEPT SUBQ /ML. This represents 2.8% of all adverse event reports for ABATACEPT SUBQ /ML.
33
Reports of Product quality issue with ABATACEPT SUBQ /ML
2.8%
of all ABATACEPT SUBQ /ML reports
0
Deaths
5
Hospitalizations
How Dangerous Is Product quality issue From ABATACEPT SUBQ /ML?
Of the 33 reports, 5 (15.2%) required hospitalization.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ABATACEPT SUBQ /ML. However, 33 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)
Incorrect product storage (45)
Fatigue (42)
Headache (41)
Nausea (36)
Sinusitis (36)
Malaise (34)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which ABATACEPT SUBQ /ML Alternatives Have Lower Product quality issue 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