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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 Abdominal discomfort? 73 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 73 reports of Abdominal discomfort have been filed in association with DEVICE. This represents 0.6% of all adverse event reports for DEVICE.

73
Reports of Abdominal discomfort with DEVICE
0.6%
of all DEVICE reports
4
Deaths
16
Hospitalizations

How Dangerous Is Abdominal discomfort From DEVICE?

Of the 73 reports, 4 (5.5%) resulted in death, 16 (21.9%) required hospitalization, and 6 (8.2%) were considered life-threatening.

Is Abdominal discomfort Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DEVICE. However, 73 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 Abdominal discomfort?

METHOTREXATE (13,237) ADALIMUMAB (12,049) ETANERCEPT (10,590) LEFLUNOMIDE (10,333) HYDROXYCHLOROQUINE (9,910) ABATACEPT (9,611) RITUXIMAB (9,591) TOCILIZUMAB (9,553) INFLIXIMAB (9,425) PREDNISONE (9,215)

Which DEVICE Alternatives Have Lower Abdominal discomfort 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 Abdominal discomfort Reports All Drugs Causing Abdominal discomfort DEVICE Demographics