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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DEVICE Cause Injection site urticaria? 37 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Injection site urticaria have been filed in association with DEVICE. This represents 0.3% of all adverse event reports for DEVICE.

37
Reports of Injection site urticaria with DEVICE
0.3%
of all DEVICE reports
0
Deaths
4
Hospitalizations

How Dangerous Is Injection site urticaria From DEVICE?

Of the 37 reports, 4 (10.8%) required hospitalization, and 3 (8.1%) were considered life-threatening.

Is Injection site urticaria Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 37 reports have been filed with the FAERS database.

What Other Side Effects Does DEVICE Cause?

Blood glucose increased (2,114) Device issue (1,417) Product use issue (1,076) Intercepted product preparation error (1,033) Wrong technique in product usage process (935) Device leakage (795) Injection site pain (751) Syringe issue (634) Product quality issue (567) Drug ineffective (488)

What Other Drugs Cause Injection site urticaria?

DUPILUMAB (3,104) ETANERCEPT (2,780) ADALIMUMAB (2,188) GLATIRAMER (1,091) TIRZEPATIDE (842) IXEKIZUMAB (652) EVOLOCUMAB (486) GALCANEZUMAB-GNLM (478) DULAGLUTIDE (450) HUMIRA (346)

Which DEVICE Alternatives Have Lower Injection site urticaria Risk?

DEVICE vs DEXAMETHASONE DEVICE vs DEXAMETHASONE\DEXAMETHASONE DEVICE vs DEXAMETHASONE\NEOMYCIN DEVICE vs DEXAMETHASONE\NEOMYCIN\POLYMYXIN B DEVICE vs DEXAMETHASONE\TOBRAMYCIN

Related Pages

DEVICE Full Profile All Injection site urticaria Reports All Drugs Causing Injection site urticaria DEVICE Demographics