Isorbide Side Effects

Report Isorbide Side Effects

If you experienced any harmful or unwanted effects of Isorbide, please share your experience. This could help to raise awareness about Isorbide side effects, identify uknown risks and inform health professionals and patients taking Isorbide.

Examples: headache, dizziness

The most commonly reported Isorbide side effects are:
Extreme Fatigue (1 reports)

If you have experienced a side effect listed above, you can check a box to report it.

To view a complete list of submitted side effects, please follow the link Isorbide side effects . You can also compare Isorbide side effects or view FDA reports.

Isorbide Side Effects reported to FDA

The following Isorbide reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
The FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

The appearance of Isorbide on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has identified a causal relationship between the drug and the listed risk.

Neutropenic Sepsis, Toxic Epidermal Necrolysis
on Sep 23, 2011 Female from UNITED KINGDOM , 57 years of age, weighting 125.7 lb, was treated with Isorbide. Directly after, patient experienced the unwanted or unexpected Isorbide side effects: neutropenic sepsis, toxic epidermal necrolysis. Isorbide dosage: N/A.
Associated medications used:
  • Ursodiol
  • Diazepam
  • Dothiepin Hydrochloride
  • Furosemide
  • Simvastatin
  • Warfarin Sodium
  • Gemcitabine Hydrochloride
  • Bisoprolol
Patient was hospitalized.

Pruritus, Blood Triglycerides Increased
Patient was taking Isorbide. Patient felt the following Isorbide side effects: pruritus, blood triglycerides increased on Dec 28, 2010 from UNITED STATES Additional patient health information: Male , weighting 285.3 lb, . Isorbide dosage: N/A.
Multiple prescriptions taken:
  • Cozaar
  • Coumadin
  • Aspirin (In The Morning)
  • Folic Acid
  • Niaspan (At Bedtime)
  • Metoprolol Tartrate

International Normalised Ratio Decreased
Adverse event was reported on Nov 05, 2010 by a Female taking Isorbide (Dosage: N/A) . Location: UNITED STATES , 77 years of age, weighting 178.6 lb, After Isorbide was administered, patient encountered several Isorbide side effects: international normalised ratio decreased.
Multiple concurrent drugs taken:
  • Omeprazole
  • Centrum Silver
  • Nifedipine
  • Vitamin B-12 (Pill And Monthly Shot)
  • Novolog (1 D.f:70/30 Units Not Specified)
  • Lorazepam
  • Lisinopril
  • Warfarin Sodium

Atrial Natriuretic Peptide Increased, Blood Chloride Decreased, Blood Sodium Decreased, Blood Urea Increased, Cardiac Failure Acute, Cardiac Failure Congestive
on Sep 26, 2006 Female from UNITED STATES , 75 years of age, weighting 133.0 lb, was diagnosed with and was treated with Isorbide. Directly after, patient experienced the unwanted or unexpected Isorbide side effects: atrial natriuretic peptide increased, blood chloride decreased, blood sodium decreased, blood urea increased, cardiac failure acute, cardiac failure congestive. Isorbide dosage: 20 Mg Tid Po. Patient was hospitalized.

Record and Track Your Side Effects

It is very important to keep track of all side effects and discuss them with your doctor. If you think you may have a medical emergency, call your doctor or 911 immediately.

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Most drugs have a large list of nonsevere or mild adverse effects which do not rule out continued usage. These effects depend on individual sensitivity, and can include nausea, dizziness, diarrhea, malaise, vomiting, headache, dermatitis, dry mouth, etc. Check commonly reported side effects . These can be considered a form of pseudo-allergic reaction, as not all users experience these effects; many users experience none at all.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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Safety Alerts, Active Ingredients, Usage Information

More About Isorbide

Side Effects reported to FDA: 4

Isorbide safety alerts: No

Reported deaths: 1

Reported hospitalizations: 2

Latest Isorbide clinical trials