PRASUGREL HYDROCHLORIDE

N/A

Manufactured by Cosette Pharmaceuticals, Inc.

14,129 FDA adverse event reports analyzed

Last updated: 2026-04-14

About PRASUGREL HYDROCHLORIDE

PRASUGREL HYDROCHLORIDE is a medication tracked in the FDA Adverse Event Reporting System (FAERS), manufactured by Cosette Pharmaceuticals, Inc.. The most commonly reported adverse reactions for PRASUGREL HYDROCHLORIDE include MYOCARDIAL INFARCTION, GASTROINTESTINAL HAEMORRHAGE, CHEST PAIN, HAEMORRHAGE, DYSPNOEA. This page provides a comprehensive breakdown of reported side effects, safety signals, patient demographics, and AI-powered safety analysis for PRASUGREL HYDROCHLORIDE.

Top Adverse Reactions

MYOCARDIAL INFARCTION503 reports
GASTROINTESTINAL HAEMORRHAGE470 reports
CHEST PAIN452 reports
HAEMORRHAGE452 reports
DYSPNOEA424 reports
CONTUSION423 reports
FATIGUE326 reports
OFF LABEL USE312 reports
NAUSEA304 reports
DIZZINESS296 reports
THROMBOSIS IN DEVICE284 reports
EPISTAXIS252 reports
HEADACHE240 reports
ASTHENIA227 reports
DEATH214 reports
RASH214 reports
FALL212 reports
DRUG INEFFECTIVE211 reports
ACUTE MYOCARDIAL INFARCTION209 reports
DIARRHOEA207 reports
DRUG DOSE OMISSION193 reports
PRURITUS186 reports
PAIN179 reports
MALAISE177 reports
HAEMORRHAGE INTRACRANIAL173 reports
ANGINA PECTORIS169 reports
VOMITING164 reports
ANAEMIA154 reports
PAIN IN EXTREMITY147 reports
CEREBROVASCULAR ACCIDENT144 reports
WEIGHT DECREASED138 reports
BACK PAIN131 reports
FLUSHING129 reports
PNEUMONIA128 reports
ARTHRALGIA126 reports
FEELING ABNORMAL122 reports
CORONARY ARTERY OCCLUSION121 reports
HYPERTENSION120 reports
ABDOMINAL PAIN UPPER117 reports
MYALGIA115 reports
HAEMOGLOBIN DECREASED114 reports
ABDOMINAL DISCOMFORT112 reports
CHEST DISCOMFORT111 reports
HAEMATOMA109 reports
VASCULAR STENT THROMBOSIS108 reports
CEREBRAL HAEMORRHAGE107 reports
CHRONIC KIDNEY DISEASE107 reports
COUGH107 reports
RENAL FAILURE106 reports
THROMBOSIS106 reports
ACUTE KIDNEY INJURY101 reports
MUSCLE SPASMS101 reports
BLOOD PRESSURE INCREASED99 reports
HYPOTENSION97 reports
CARDIAC DISORDER96 reports
CORONARY ARTERY DISEASE94 reports
ANXIETY93 reports
URTICARIA93 reports
ABDOMINAL PAIN92 reports
DEVICE OCCLUSION90 reports
GAIT DISTURBANCE90 reports
RECTAL HAEMORRHAGE90 reports
INSOMNIA88 reports
ATRIAL FIBRILLATION86 reports
HYPERSENSITIVITY86 reports
BLOOD GLUCOSE INCREASED85 reports
DECREASED APPETITE85 reports
PYREXIA84 reports
CARDIAC FAILURE CONGESTIVE82 reports
HOSPITALISATION82 reports
STENT PLACEMENT82 reports
CARDIAC FAILURE81 reports
PARAESTHESIA78 reports
DEPRESSION77 reports
HYPOAESTHESIA77 reports
INTENTIONAL PRODUCT MISUSE77 reports
ERYTHEMA73 reports
SYNCOPE72 reports
TRANSIENT ISCHAEMIC ATTACK71 reports
CONSTIPATION70 reports
LOSS OF CONSCIOUSNESS70 reports
PLATELET COUNT DECREASED70 reports
SUBDURAL HAEMATOMA70 reports
CARDIAC ARREST69 reports
DRUG INTERACTION69 reports
CEREBRAL INFARCTION68 reports
DEHYDRATION68 reports
DYSPEPSIA68 reports
WEIGHT INCREASED68 reports
ANGINA UNSTABLE67 reports
THROMBOCYTOPENIA67 reports
VISION BLURRED65 reports
URINARY TRACT INFECTION63 reports
BLOOD PRESSURE DECREASED62 reports
HAEMATURIA62 reports
PERIPHERAL SWELLING62 reports
MUSCULAR WEAKNESS61 reports
HAEMOPTYSIS59 reports
OEDEMA PERIPHERAL59 reports
GASTROOESOPHAGEAL REFLUX DISEASE58 reports

Report Outcomes

Out of 9,953 classified reports for PRASUGREL HYDROCHLORIDE:

Serious 74.9%Non-Serious 25.1%

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

Male6,116 (64.6%)
Female3,310 (35.0%)
Unknown38 (0.4%)

Reports by Age

Age 65265 reports
Age 60239 reports
Age 55230 reports
Age 70228 reports
Age 75195 reports
Age 69189 reports
Age 67188 reports
Age 66187 reports
Age 62182 reports
Age 64177 reports
Age 61170 reports
Age 72168 reports
Age 59162 reports
Age 71162 reports
Age 63154 reports
Age 68147 reports
Age 73144 reports
Age 57137 reports
Age 58137 reports
Age 50128 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 PRASUGREL HYDROCHLORIDE?

This profile reflects 14,129 FDA FAERS reports that mention PRASUGREL HYDROCHLORIDE. Reporting is voluntary and does not prove that the drug caused any listed event.

Which adverse reactions are most often listed for PRASUGREL HYDROCHLORIDE?

Frequently reported terms in FAERS include MYOCARDIAL INFARCTION, GASTROINTESTINAL HAEMORRHAGE, CHEST PAIN, HAEMORRHAGE, DYSPNOEA, CONTUSION. Rankings reflect reporting volume in this dataset, not confirmed side effect rates in the general population.

Who manufactures PRASUGREL HYDROCHLORIDE?

Labeling and FAERS entries often list Cosette Pharmaceuticals, Inc. in connection with PRASUGREL HYDROCHLORIDE. 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.