Does ISOSORBIDE MONONITRATE Cause Product administration error? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product administration error have been filed in association with ISOSORBIDE MONONITRATE (Isosorbide Mononitrate). This represents 0.5% of all adverse event reports for ISOSORBIDE MONONITRATE.
12
Reports of Product administration error with ISOSORBIDE MONONITRATE
0.5%
of all ISOSORBIDE MONONITRATE reports
1
Deaths
12
Hospitalizations
How Dangerous Is Product administration error From ISOSORBIDE MONONITRATE?
Of the 12 reports, 1 (8.3%) resulted in death, 12 (100.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ISOSORBIDE MONONITRATE. However, 12 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 Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which ISOSORBIDE MONONITRATE Alternatives Have Lower Product administration error Risk?
ISOSORBIDE MONONITRATE vs ISOTRETINOIN
ISOSORBIDE MONONITRATE vs ISRADIPINE
ISOSORBIDE MONONITRATE vs ISTRADEFYLLINE
ISOSORBIDE MONONITRATE vs ITACITINIB
ISOSORBIDE MONONITRATE vs ITRACONAZOLE