TRIMETHOPRIM

N/A

Manufactured by Dr. Reddy's Labratories Inc.

33,626 FDA adverse event reports analyzed

Last updated: 2026-04-14

About TRIMETHOPRIM

TRIMETHOPRIM is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Dr. Reddy's Labratories Inc.. The most commonly reported adverse reactions for TRIMETHOPRIM include NAUSEA, OFF LABEL USE, DIARRHOEA, HEADACHE, MALAISE. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for TRIMETHOPRIM.

Top Adverse Reactions

NAUSEA945 reports
OFF LABEL USE868 reports
DIARRHOEA848 reports
HEADACHE835 reports
MALAISE814 reports
DRUG INEFFECTIVE746 reports
PYREXIA722 reports
DYSPNOEA712 reports
VOMITING707 reports
FATIGUE641 reports
PAIN605 reports
RASH605 reports
DIZZINESS599 reports
ACUTE KIDNEY INJURY594 reports
URINARY TRACT INFECTION554 reports
ARTHRALGIA549 reports
ABDOMINAL PAIN496 reports
HYPERSENSITIVITY472 reports
CONFUSIONAL STATE463 reports
PERIPHERAL SWELLING438 reports
DRUG INTOLERANCE435 reports
PRURITUS432 reports
DRUG INTERACTION423 reports
PNEUMONIA418 reports
CONDITION AGGRAVATED411 reports
INFECTION407 reports
SWELLING FACE400 reports
DRUG HYPERSENSITIVITY395 reports
JOINT SWELLING384 reports
ASTHENIA383 reports
WEIGHT DECREASED347 reports
ANXIETY336 reports
BACK PAIN334 reports
CONSTIPATION330 reports
DECREASED APPETITE327 reports
ANAEMIA325 reports
INSOMNIA324 reports
LOWER RESPIRATORY TRACT INFECTION306 reports
ABDOMINAL PAIN UPPER302 reports
PAIN IN EXTREMITY296 reports
PRODUCT USE IN UNAPPROVED INDICATION296 reports
HYPERTENSION283 reports
SWOLLEN TONGUE281 reports
FALL279 reports
FIBROMYALGIA271 reports
PARAESTHESIA270 reports
HYPONATRAEMIA269 reports
SWELLING269 reports
URTICARIA263 reports
CHRONIC KIDNEY DISEASE262 reports
ANGIOEDEMA249 reports
CHEST PAIN249 reports
CONTUSION249 reports
WHEEZING244 reports
DEATH242 reports
INFUSION RELATED REACTION236 reports
DYSPHONIA234 reports
FEBRILE NEUTROPENIA234 reports
HYPOTENSION233 reports
SYNOVITIS231 reports
ABDOMINAL DISCOMFORT230 reports
THERAPEUTIC PRODUCT EFFECT INCOMPLETE229 reports
TREMOR229 reports
MUSCULOSKELETAL STIFFNESS226 reports
COUGH223 reports
RENAL FAILURE222 reports
ERYTHEMA219 reports
INFLAMMATION219 reports
BLOOD CHOLESTEROL INCREASED218 reports
MUSCULAR WEAKNESS218 reports
FEELING ABNORMAL214 reports
RHEUMATOID ARTHRITIS213 reports
HYPERKALAEMIA209 reports
NEUTROPENIA208 reports
GENERAL PHYSICAL HEALTH DETERIORATION206 reports
MUSCLE SPASMS204 reports
DRY MOUTH203 reports
ARTHRITIS198 reports
MUSCULOSKELETAL PAIN198 reports
ALOPECIA196 reports
HYPOAESTHESIA195 reports
C REACTIVE PROTEIN INCREASED192 reports
MYALGIA192 reports
NASOPHARYNGITIS192 reports
STOMATITIS192 reports
LIVER FUNCTION TEST ABNORMAL189 reports
WEIGHT INCREASED188 reports
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION186 reports
LEUKOPENIA184 reports
GASTROINTESTINAL DISORDER183 reports
THROMBOCYTOPENIA183 reports
RECTAL HAEMORRHAGE180 reports
SOMNOLENCE180 reports
SINUSITIS179 reports
HAEMOGLOBIN DECREASED178 reports
SEPSIS178 reports
ARTHROPATHY177 reports
LUNG DISORDER177 reports
DYSPEPSIA174 reports
PALPITATIONS173 reports

Report Outcomes

Out of 11,380 classified reports for TRIMETHOPRIM:

Serious 91.7%Non-Serious 8.3%

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

Female6,999 (68.0%)
Male3,221 (31.3%)
Unknown74 (0.7%)

Reports by Age

Age 44293 reports
Age 78266 reports
Age 41250 reports
Age 76249 reports
Age 71248 reports
Age 74238 reports
Age 75228 reports
Age 67209 reports
Age 73198 reports
Age 69196 reports
Age 79190 reports
Age 68173 reports
Age 77169 reports
Age 65168 reports
Age 70165 reports
Age 60160 reports
Age 83160 reports
Age 62154 reports
Age 64153 reports
Age 72146 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 TRIMETHOPRIM?

This profile reflects 33,626 FDA FAERS reports that mention TRIMETHOPRIM. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for TRIMETHOPRIM?

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

Who manufactures TRIMETHOPRIM?

Labeling and FAERS entries often list Dr. Reddy's Labratories Inc. in connection with TRIMETHOPRIM. 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.