PYRIDOSTIGMINE BROMIDE

N/A

16,739 FDA adverse event reports analyzed

Last updated: 2026-04-15

About PYRIDOSTIGMINE BROMIDE

PYRIDOSTIGMINE BROMIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS). The most commonly reported adverse reactions for PYRIDOSTIGMINE BROMIDE include MYASTHENIA GRAVIS, FATIGUE, DRUG INEFFECTIVE, ASTHENIA, OFF LABEL USE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PYRIDOSTIGMINE BROMIDE.

Top Adverse Reactions

MYASTHENIA GRAVIS792 reports
FATIGUE667 reports
DRUG INEFFECTIVE551 reports
ASTHENIA525 reports
OFF LABEL USE524 reports
DIARRHOEA502 reports
DYSPNOEA475 reports
HEADACHE474 reports
NAUSEA420 reports
MUSCULAR WEAKNESS360 reports
FALL337 reports
DIZZINESS305 reports
MALAISE283 reports
PAIN275 reports
DIPLOPIA274 reports
DYSPHAGIA252 reports
VOMITING238 reports
CONDITION AGGRAVATED236 reports
ARTHRALGIA226 reports
PYREXIA214 reports
PNEUMONIA197 reports
URINARY TRACT INFECTION193 reports
PRODUCT DOSE OMISSION ISSUE192 reports
GAIT DISTURBANCE190 reports
COVID 19189 reports
BLOOD PRESSURE INCREASED186 reports
WEIGHT DECREASED183 reports
MUSCLE SPASMS173 reports
PARAESTHESIA170 reports
DEATH169 reports
FEELING ABNORMAL169 reports
EYELID PTOSIS167 reports
BACK PAIN162 reports
COUGH160 reports
PAIN IN EXTREMITY160 reports
RASH159 reports
ABDOMINAL PAIN UPPER157 reports
MYASTHENIA GRAVIS CRISIS156 reports
WEIGHT INCREASED149 reports
INTENTIONAL PRODUCT USE ISSUE145 reports
INSOMNIA139 reports
PRODUCT USE IN UNAPPROVED INDICATION132 reports
SOMNOLENCE129 reports
HYPOTENSION128 reports
MYALGIA125 reports
ANXIETY124 reports
NASOPHARYNGITIS120 reports
DEPRESSION116 reports
HYPERTENSION114 reports
PRURITUS114 reports
ABDOMINAL DISCOMFORT113 reports
VISION BLURRED113 reports
ABDOMINAL PAIN111 reports
HYPOAESTHESIA111 reports
INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION109 reports
CHILLS101 reports
HYPERHIDROSIS101 reports
TREMOR101 reports
BALANCE DISORDER98 reports
SPEECH DISORDER98 reports
DECREASED APPETITE97 reports
URTICARIA97 reports
DYSARTHRIA96 reports
SINUSITIS92 reports
INFECTION90 reports
RESPIRATORY FAILURE90 reports
THERAPEUTIC RESPONSE SHORTENED90 reports
ANAEMIA89 reports
PERIPHERAL SWELLING89 reports
CONFUSIONAL STATE87 reports
CONSTIPATION87 reports
GASTROINTESTINAL DISORDER87 reports
INFLUENZA87 reports
HOSPITALISATION85 reports
VISUAL IMPAIRMENT85 reports
DRUG INTERACTION84 reports
LOSS OF CONSCIOUSNESS82 reports
MIGRAINE79 reports
DEHYDRATION77 reports
SEPSIS77 reports
CHEST PAIN75 reports
STRESS73 reports
PARAESTHESIA ORAL72 reports
CONTUSION70 reports
ERYTHEMA70 reports
INFUSION RELATED REACTION69 reports
INJECTION SITE PAIN68 reports
ILLNESS67 reports
PRODUCT SUBSTITUTION ISSUE67 reports
ATRIAL FIBRILLATION66 reports
HALLUCINATION66 reports
OXYGEN SATURATION DECREASED66 reports
CELLULITIS65 reports
HYPERSENSITIVITY65 reports
PALPITATIONS65 reports
MUSCULOSKELETAL STIFFNESS64 reports
INCORRECT DOSE ADMINISTERED63 reports
NECK PAIN63 reports
SYMPTOM RECURRENCE63 reports
DYSPHONIA62 reports

Demographics Breakdown

Reports by Sex

Female3,671 (61.0%)
Male2,338 (38.9%)
Unknown5 (0.1%)

Demographics reflect voluntary FDA adverse event reporting patterns and may not represent the full patient population.

Frequently Asked Questions

How many FDA adverse event reports are associated with PYRIDOSTIGMINE BROMIDE?

This profile reflects 16,739 FDA FAERS reports that mention PYRIDOSTIGMINE BROMIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PYRIDOSTIGMINE BROMIDE?

Frequently reported terms in FAERS include MYASTHENIA GRAVIS, FATIGUE, DRUG INEFFECTIVE, ASTHENIA, OFF LABEL USE, DIARRHOEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Important Disclaimer: This content is generated by AI analysis of FDA adverse event reports and is provided for informational purposes only. It is not medical advice. Adverse event reports submitted to the FDA do not prove that a medication caused the reported side effect. Always consult your healthcare provider before starting, stopping, or changing any medication. If you experience a serious side effect, contact your doctor or call 911 immediately.