Does ISOSORBIDE MONONITRATE Cause Intentional product use issue? 283 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 283 reports of Intentional product use issue have been filed in association with ISOSORBIDE MONONITRATE (Isosorbide Mononitrate). This represents 11.0% of all adverse event reports for ISOSORBIDE MONONITRATE.
283
Reports of Intentional product use issue with ISOSORBIDE MONONITRATE
11.0%
of all ISOSORBIDE MONONITRATE reports
0
Deaths
100
Hospitalizations
How Dangerous Is Intentional product use issue From ISOSORBIDE MONONITRATE?
Of the 283 reports, 100 (35.3%) required hospitalization, and 76 (26.9%) 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 ISOSORBIDE MONONITRATE. However, 283 reports have been filed with the FAERS database.
What Other Side Effects Does ISOSORBIDE MONONITRATE Cause?
Dizziness (554)
Headache (500)
Dyspnoea (462)
Chest pain (458)
Nausea (458)
Fatigue (446)
Diarrhoea (439)
Pruritus (416)
Myocardial infarction (409)
Malaise (405)
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 ISOSORBIDE MONONITRATE Alternatives Have Lower Intentional product use issue Risk?
ISOSORBIDE MONONITRATE vs ISOTRETINOIN
ISOSORBIDE MONONITRATE vs ISRADIPINE
ISOSORBIDE MONONITRATE vs ISTRADEFYLLINE
ISOSORBIDE MONONITRATE vs ITACITINIB
ISOSORBIDE MONONITRATE vs ITRACONAZOLE