Does ISOSORBIDE MONONITRATE Cause Incorrect product administration duration? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Incorrect product administration duration have been filed in association with ISOSORBIDE MONONITRATE (Isosorbide Mononitrate). This represents 1.0% of all adverse event reports for ISOSORBIDE MONONITRATE.
26
Reports of Incorrect product administration duration with ISOSORBIDE MONONITRATE
1.0%
of all ISOSORBIDE MONONITRATE reports
0
Deaths
26
Hospitalizations
How Dangerous Is Incorrect product administration duration From ISOSORBIDE MONONITRATE?
Of the 26 reports, 26 (100.0%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ISOSORBIDE MONONITRATE. However, 26 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which ISOSORBIDE MONONITRATE Alternatives Have Lower Incorrect product administration duration Risk?
ISOSORBIDE MONONITRATE vs ISOTRETINOIN
ISOSORBIDE MONONITRATE vs ISRADIPINE
ISOSORBIDE MONONITRATE vs ISTRADEFYLLINE
ISOSORBIDE MONONITRATE vs ITACITINIB
ISOSORBIDE MONONITRATE vs ITRACONAZOLE