INDAPAMIDE

N/A

Manufactured by ANI Pharmaceuticals, Inc.

35,549 FDA adverse event reports analyzed

Last updated: 2026-04-14

About INDAPAMIDE

INDAPAMIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by ANI Pharmaceuticals, Inc.. The most commonly reported adverse reactions for INDAPAMIDE include HYPONATRAEMIA, ACUTE KIDNEY INJURY, DYSPNOEA, DIZZINESS, NAUSEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for INDAPAMIDE.

Top Adverse Reactions

HYPONATRAEMIA1,286 reports
ACUTE KIDNEY INJURY925 reports
DYSPNOEA899 reports
DIZZINESS876 reports
NAUSEA863 reports
DIARRHOEA843 reports
FATIGUE782 reports
DRUG INTERACTION756 reports
HYPOKALAEMIA746 reports
VOMITING699 reports
MALAISE695 reports
DRUG INEFFECTIVE660 reports
FALL653 reports
ASTHENIA640 reports
HEADACHE640 reports
OFF LABEL USE614 reports
ARTHRALGIA608 reports
HYPOTENSION596 reports
CONFUSIONAL STATE571 reports
COUGH564 reports
PAIN535 reports
HYPERTENSION508 reports
RASH492 reports
BLOOD PRESSURE INCREASED469 reports
ABDOMINAL PAIN433 reports
PAIN IN EXTREMITY430 reports
PYREXIA399 reports
WEIGHT DECREASED398 reports
OEDEMA PERIPHERAL397 reports
ATRIAL FIBRILLATION390 reports
PNEUMONIA388 reports
DECREASED APPETITE383 reports
MYALGIA376 reports
CONDITION AGGRAVATED371 reports
PRURITUS352 reports
JOINT SWELLING346 reports
DEHYDRATION337 reports
ANAEMIA336 reports
CHEST PAIN336 reports
GAIT DISTURBANCE335 reports
PERIPHERAL SWELLING331 reports
BACK PAIN319 reports
SYNCOPE308 reports
INSOMNIA305 reports
CONSTIPATION303 reports
SOMNOLENCE297 reports
BRADYCARDIA296 reports
URINARY TRACT INFECTION283 reports
RENAL FAILURE278 reports
ABDOMINAL PAIN UPPER272 reports
ANXIETY270 reports
BLOOD CREATININE INCREASED257 reports
MUSCLE SPASMS255 reports
HAEMOGLOBIN DECREASED248 reports
RENAL IMPAIRMENT237 reports
INFLUENZA232 reports
MUSCULAR WEAKNESS230 reports
OROPHARYNGEAL PAIN227 reports
CHEST DISCOMFORT224 reports
FEELING ABNORMAL222 reports
HYPOMAGNESAEMIA222 reports
ASTHMA219 reports
NASOPHARYNGITIS219 reports
HYPERHIDROSIS216 reports
WEIGHT INCREASED213 reports
LOSS OF CONSCIOUSNESS211 reports
PARAESTHESIA207 reports
BLOOD GLUCOSE INCREASED206 reports
WHEEZING201 reports
DIABETES MELLITUS198 reports
GENERAL PHYSICAL HEALTH DETERIORATION196 reports
DEATH195 reports
CEREBROVASCULAR ACCIDENT192 reports
HYPERKALAEMIA189 reports
RHABDOMYOLYSIS187 reports
MYOCARDIAL INFARCTION185 reports
PALPITATIONS184 reports
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION181 reports
ABDOMINAL DISCOMFORT180 reports
HYPOAESTHESIA179 reports
TREMOR179 reports
CARDIAC FAILURE176 reports
LACTIC ACIDOSIS172 reports
HYPOGLYCAEMIA171 reports
RENAL FAILURE ACUTE171 reports
ERYTHEMA170 reports
DYSPHAGIA168 reports
HYPERSENSITIVITY167 reports
ELECTROCARDIOGRAM QT PROLONGED165 reports
VISION BLURRED162 reports
ANGIOEDEMA160 reports
COVID 19159 reports
DEPRESSION158 reports
CONTUSION157 reports
ARTHRITIS155 reports
ARRHYTHMIA153 reports
BLOOD PRESSURE SYSTOLIC INCREASED153 reports
THROMBOCYTOPENIA153 reports
DYSPNOEA EXERTIONAL150 reports
MOBILITY DECREASED149 reports

Report Outcomes

Out of 17,198 classified reports for INDAPAMIDE:

Serious 92.6%Non-Serious 7.4%

The FDA classifies an adverse event as “serious” if it results in death, hospitalization, disability, congenital anomaly, or requires intervention to prevent permanent damage.

Demographics Breakdown

Reports by Sex

Female9,088 (57.5%)
Male6,694 (42.4%)
Unknown19 (0.1%)

Reports by Age

Age 69508 reports
Age 72498 reports
Age 71492 reports
Age 68458 reports
Age 73453 reports
Age 65445 reports
Age 67423 reports
Age 75417 reports
Age 63416 reports
Age 70410 reports
Age 76410 reports
Age 74399 reports
Age 77393 reports
Age 62375 reports
Age 78371 reports
Age 80353 reports
Age 66342 reports
Age 64332 reports
Age 55319 reports
Age 82300 reports

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 INDAPAMIDE?

This profile reflects 35,549 FDA FAERS reports that mention INDAPAMIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for INDAPAMIDE?

Frequently reported terms in FAERS include HYPONATRAEMIA, ACUTE KIDNEY INJURY, DYSPNOEA, DIZZINESS, NAUSEA, DIARRHOEA. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures INDAPAMIDE?

Labeling and FAERS entries often list ANI Pharmaceuticals, Inc. in connection with INDAPAMIDE. Always verify the specific product and NDC with your pharmacist.

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.