Does SULFISOMIDINE Cause Intentional product use issue? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Intentional product use issue have been filed in association with SULFISOMIDINE. This represents 9.7% of all adverse event reports for SULFISOMIDINE.
26
Reports of Intentional product use issue with SULFISOMIDINE
9.7%
of all SULFISOMIDINE reports
26
Deaths
21
Hospitalizations
How Dangerous Is Intentional product use issue From SULFISOMIDINE?
Of the 26 reports, 26 (100.0%) resulted in death, 21 (80.8%) required hospitalization, and 17 (65.4%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SULFISOMIDINE. However, 26 reports have been filed with the FAERS database.
What Other Side Effects Does SULFISOMIDINE Cause?
Hypertension (148)
Hypoaesthesia (145)
Helicobacter infection (132)
Infusion related reaction (132)
General physical health deterioration (126)
Headache (126)
Hypercholesterolaemia (124)
Fibromyalgia (123)
Osteoarthritis (122)
Hepatic enzyme increased (121)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which SULFISOMIDINE Alternatives Have Lower Intentional product use issue Risk?
SULFISOMIDINE vs SULFUR
SULFISOMIDINE vs SULFUR HEXAFLUORIDE
SULFISOMIDINE vs SULINDAC
SULFISOMIDINE vs SULPIRIDE
SULFISOMIDINE vs SULTAMICILLIN