Isosorbide mononitrate adverse reactions: Difference between revisions

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The table below shows the frequencies of the adverse events that occurred in >5% of the subjects in three placebo-controlled North American studies, in which patients in the active treatment arm received 30 mg, 60 mg, 120 mg, or 240 mg of ISMN as Isosorbide mononitrate extended-release tablets once daily. In parentheses, the same table shows the frequencies with which these adverse events were associated with the discontinuation of treatment. Overall, 8% of the patients who received 30 mg, 60 mg, 120 mg, or 240 mg of ISMN in the three placebo-controlled North American studies discontinued treatment because of adverse events. Most of these discontinued because of headache. Dizziness was rarely associated with withdrawal from these studies. Since headache appears to be a dose-related adverse effect and tends to disappear with continued treatment, it is recommended that Isosorbide mononitrate extended-release tablets treatment be initiated at low doses for several days before being increased to desired levels.


FREQUENCY AND ADVERSE EVENTS (DISCONTINUED)


In addition, the three North American trials were pooled with 11 controlled trials conducted in Europe. Among the 14 controlled trials, a total of 711 patients were randomized to Isosorbide mononitrate extended-release tablets. When the pooled data were reviewed, headache and dizziness were the only adverse events that were reported by >5% of patients. Other adverse events, each reported by ≤ 5% of exposed patients, and in many cases of uncertain relation to drug treatment, were:
* Autonomic Nervous System Disorders: [[Dry mouth]], [[hot flushes]].
* Body As A Whole: [[Asthenia]], back pain, [[chest pain]], [[edema]], [[fatigue]], [[fever]], flu-like symptoms, [[malaise]], [[rigor]]s.
* Cardiovascular Disorders, General: [[Cardiac failure]], [[hypertension]], [[hypotension]].
* Central And Peripheral Nervous System Disorders: [[Dizziness]], [[headache]], [[hypoesthesia]], [[migraine]], [[neuritis]], [[paresis]], [[paresthesia]], [[ptosis]], [[tremor]], [[vertigo]].
* Gastrointestinal System Disorders: [[Abdominal pain]], [[constipation]], [[diarrhea]], [[dyspepsia]], [[flatulence]], [[gastric ulcer]], [[gastritis]], [[glossitis]], hemorrhagic [[gastric ulcer]], [[hemorrhoid]]s, loose stools, [[melena]], [[nausea]], [[vomiting]].
* Hearing And Vestibular Disorders: Earache, [[tinnitus]], tympanic membrane perforation.
* Heart Rate and Rhythm Disorders: [[Arrhythmia]], [[arrhythmia]] atrial, [[atrial fibrillation]], [[bradycardia]], [[bundle branch block]], [[extrasystole]], [[palpitation]], [[tachycardia]], [[ventricular tachycardia]].
* Liver and Biliary System Disorders: SGOT increase, SGPT increase.
* Metabolic and Nutritional Disorders: [[Hyperuricemia]], [[hypokalemia]].
* Musculoskeletal System Disorders: [[Arthralgia]], [[frozen shoulder]], muscle weakness, musculoskeletal pain, [[myalgia]], [[myositis]], tendon disorder, [[torticollis]].
* Myo-, Endo-, Pericardial and Valve Disorders: [[Angina pectoris]] aggravated, [[heart murmur]], heart sound abnormal, [[myocardial infarction]], Q-Waveabnormality.
* Platelet: Bleeding, And Clotting Disorders: [[Purpura]], [[thrombocytopenia]].
* Psychiatric Disorders: [[Anxiety]], concentration impaired, [[confusion]], decreased libido, [[depression]], [[impotence]], [[insomnia]], [[nervousness]], paroniria, [[somnolence]].
* Red Blood Cell Disorder: [[Hypochromic anemia]].
* Reproductive Disorders, Female: [[Atrophic vaginitis]], [[breast pain]].
* Resistance Mechanism Disorders: Bacterial infection, [[moniliasis]], [[viral infection]].
* Respiratory System Disorders: [[Bronchitis]], [[bronchospasm]], [[coughing]], [[dyspnea]], increased sputum, nasal congestion, [[pharyngitis]], [[pneumonia]], pulmonary infiltration, [[rales]], [[rhinitis]], [[sinusitis]].
* Skin and Appendages Disorders: [[Acne]], hair texture abnormal, increased sweating, [[pruritus]], [[rash]], skin nodule.
* Urinary System Disorders: [[Polyuria]], [[renal calculus]], [[urinary tract infection]].
* Vascular (Extracardiac) Disorders: [[Flushing]], [[intermittent claudication]], leg ulcer, [[varicose vein]].
* Vision Disorders: [[Conjunctivitis]], [[photophobia]], vision abnormal.
In addition, the following spontaneous adverse event has been reported during the marketing of Isosorbide Mononitrate (ISMN): [[syncope]].


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Revision as of 19:48, 30 January 2014

Isosorbide mononitrate
ISOSORBIDE MONONITRATE tablet® FDA Package Insert
Indications and Usage
Dosage and Administration
Dosage Forms and Strengths
Contraindications
Warnings and Precautions
Adverse Reactions
Drug Interactions
Overdosage
Description
Clinical Pharmacology
Clinical Studies
How Supplied/Storage and Handling
Patient Counseling Information
Labels and Packages
Clinical Trials
ClinicalTrials.gov

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Pratik Bahekar, MBBS [2]

The table below shows the frequencies of the adverse events that occurred in >5% of the subjects in three placebo-controlled North American studies, in which patients in the active treatment arm received 30 mg, 60 mg, 120 mg, or 240 mg of ISMN as Isosorbide mononitrate extended-release tablets once daily. In parentheses, the same table shows the frequencies with which these adverse events were associated with the discontinuation of treatment. Overall, 8% of the patients who received 30 mg, 60 mg, 120 mg, or 240 mg of ISMN in the three placebo-controlled North American studies discontinued treatment because of adverse events. Most of these discontinued because of headache. Dizziness was rarely associated with withdrawal from these studies. Since headache appears to be a dose-related adverse effect and tends to disappear with continued treatment, it is recommended that Isosorbide mononitrate extended-release tablets treatment be initiated at low doses for several days before being increased to desired levels.

FREQUENCY AND ADVERSE EVENTS (DISCONTINUED)

In addition, the three North American trials were pooled with 11 controlled trials conducted in Europe. Among the 14 controlled trials, a total of 711 patients were randomized to Isosorbide mononitrate extended-release tablets. When the pooled data were reviewed, headache and dizziness were the only adverse events that were reported by >5% of patients. Other adverse events, each reported by ≤ 5% of exposed patients, and in many cases of uncertain relation to drug treatment, were:

In addition, the following spontaneous adverse event has been reported during the marketing of Isosorbide Mononitrate (ISMN): syncope.

[1]

References

  1. "ISOSORBIDE MONONITRATE TABLET [ZYDUS PHARMACEUTICALS (USA) INC.]". Retrieved 30 January 2014.