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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 Needle issue? 110 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 110 reports of Needle issue have been filed in association with DEVICE. This represents 0.9% of all adverse event reports for DEVICE.

110
Reports of Needle issue with DEVICE
0.9%
of all DEVICE reports
0
Deaths
8
Hospitalizations

How Dangerous Is Needle issue From DEVICE?

Of the 110 reports, 8 (7.3%) required hospitalization, and 2 (1.8%) were considered life-threatening.

Is Needle issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 110 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 Needle issue?

OCTREOTIDE (2,740) GUSELKUMAB (1,933) USTEKINUMAB (1,930) EXENATIDE (1,821) GOLIMUMAB (1,023) ADALIMUMAB (1,022) SOMATROPIN (981) SECUKINUMAB (958) ABATACEPT (716) DUPILUMAB (686)

Which DEVICE Alternatives Have Lower Needle issue 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 Needle issue Reports All Drugs Causing Needle issue DEVICE Demographics