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Simvastatin and Aspirin

Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side EffectSimvastatinAspirin
FATIGUE2.9% 2.9%
NAUSEA2.8% 2.9%
DYSPNOEA2.9% 2.8%
DRUG INEFFECTIVE2.7% 2.2%
DIARRHOEA2.5% 2.4%
DIZZINESS2.5% 2.4%
FALL2.1% 1.8%
ASTHENIA2% 2%
HEADACHE1.9% 2%
PAIN1.9% 1.8%
MYOCARDIAL INFARCTION1% 1.9%
MYALGIA1.9% 0.9%
DRUG INTERACTION1.9% 0.9%
VOMITING1.8% 1.8%
MALAISE1.8% 1.4%
PAIN IN EXTREMITY1.7% 1.4%
GASTROINTESTINAL HAEMORRHAGE1% 1.7%
FLUSHING0.9% 1.7%
ARTHRALGIA1.6% 1.4%
PNEUMONIA1.4% 1.6%
CHEST PAIN1.2% 1.4%
PRURITUS1.2% 1.4%
ANAEMIA1.1% 1.4%
DEATH1.1% 1.4%
PYREXIA1% 1.4%
WEIGHT DECREASED1.3% 1.3%
HYPOTENSION1.2% 1.3%
CEREBROVASCULAR ACCIDENT0.9% 1.3%
RHABDOMYOLYSIS1.3% 0%
RASH1.2% 1.2%
INSOMNIA1.2% 1%
HYPERTENSION1% 1.2%
CONFUSIONAL STATE1.2% 0.9%
COUGH1.1% 1.1%
OFF LABEL USE1.1% 1%
BACK PAIN1% 1.1%
GAIT DISTURBANCE1.1% 0.8%
CARDIAC FAILURE CONGESTIVE0.6% 1.1%
DECREASED APPETITE1% 1%
ANXIETY0.9% 1%
BLOOD GLUCOSE INCREASED1% 0.9%
ABDOMINAL PAIN0.9% 1%
OEDEMA PERIPHERAL0.9% 1%
DEPRESSION1% 0.9%
CONSTIPATION0.9% 1%
RENAL FAILURE ACUTE1% 0.8%
MUSCLE SPASMS1% 0.8%
ACUTE KIDNEY INJURY1% 0.6%
MUSCULAR WEAKNESS1% 0.6%
RENAL FAILURE0.9% 0.9%
PARAESTHESIA0.8% 0.9%
DEHYDRATION0.9% 0.8%
FEELING ABNORMAL0.9% 0.8%
ATRIAL FIBRILLATION0.8% 0.9%
URINARY TRACT INFECTION0.8% 0.8%
SOMNOLENCE0.8% 0.8%
CONDITION AGGRAVATED0.8% 0.8%
ABDOMINAL PAIN UPPER0.8% 0.8%
SYNCOPE0.8% 0.7%
BLOOD PRESSURE INCREASED0.7% 0.8%
DRUG DOSE OMISSION0.8% 0.6%
HAEMOGLOBIN DECREASED0.6% 0.8%
TOXICITY TO VARIOUS AGENTS0% 0.8%
COMPLETED SUICIDE0% 0.8%
WEIGHT INCREASED0.7% 0.7%
LOSS OF CONSCIOUSNESS0.7% 0.7%
TREMOR0.7% 0.7%
HYPERHIDROSIS0.7% 0.6%
ERYTHEMA0.6% 0.7%
HYPOAESTHESIA0.7% 0.6%
CORONARY ARTERY DISEASE0% 0.7%
ABDOMINAL DISCOMFORT0.6% 0.6%
SEPSIS0.6% 0.6%
CONTUSION0.5% 0.6%
DRUG HYPERSENSITIVITY0.5% 0.6%
EPISTAXIS0.5% 0.6%
THROMBOCYTOPENIA0.4% 0.6%
MEMORY IMPAIRMENT0.6% 0%
CARDIAC ARREST0% 0.6%
BALANCE DISORDER0.6% 0%
INJECTION SITE PAIN0.6% 0%
ALOPECIA0.6% 0%
OVERDOSE0% 0.6%
BLOOD CREATINE PHOSPHOKINASE INCREASED0.6% 0%
HAEMORRHAGE0% 0.6%
FEELING HOT0% 0.6%
GENERAL PHYSICAL HEALTH DETERIORATION0.6% 0%
HYPERSENSITIVITY0.5% 0.5%
VISION BLURRED0.5% 0.5%
DYSPEPSIA0.5% 0.5%
NASOPHARYNGITIS0.5% 0.5%
PERIPHERAL SWELLING0.5% 0.5%
PALPITATIONS0.5% 0.5%
BLOOD CREATININE INCREASED0.5% 0.5%
HEART RATE INCREASED0% 0.5%
CHILLS0% 0.5%
CHEST DISCOMFORT0% 0.5%
ACUTE MYOCARDIAL INFARCTION0% 0.5%
PLATELET COUNT DECREASED0% 0.5%
URTICARIA0% 0.5%
RECTAL HAEMORRHAGE0% 0.5%
CARDIAC DISORDER0% 0.5%
GASTROOESOPHAGEAL REFLUX DISEASE0% 0.5%
HYPONATRAEMIA0.5% 0%
RESPIRATORY FAILURE0% 0.5%
DIABETES MELLITUS0.5% 0%
PULMONARY EMBOLISM0% 0.5%
HYPOGLYCAEMIA0.5% 0%
RENAL IMPAIRMENT0.5% 0%
PRODUCT QUALITY ISSUE0.5% 0%
DYSPHAGIA0.4% 0.4%
AMNESIA0.4% 0%
JOINT SWELLING0.4% 0%
INTERNATIONAL NORMALISED RATIO INCREASED0.4% 0%
CHRONIC KIDNEY DISEASE0.4% 0%
INCORRECT DOSE ADMINISTERED0.4% 0%
BRADYCARDIA0.4% 0%
CARDIAC FAILURE0.4% 0%
ALANINE AMINOTRANSFERASE INCREASED0% 0.4%

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