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Simvastatin and Bactrim

Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side EffectSimvastatinBactrim
PYREXIA1% 3.8%
NAUSEA2.8% 3%
FATIGUE2.9% 2.4%
DYSPNOEA2.9% 2.2%
DIARRHOEA2.5% 2.8%
DRUG INEFFECTIVE2.7% 1.3%
DIZZINESS2.5% 1.3%
VOMITING1.8% 2.4%
DRUG HYPERSENSITIVITY0.5% 2.4%
RASH1.2% 2.1%
FALL2.1% 1%
ASTHENIA2% 1.8%
PNEUMONIA1.4% 2%
HEADACHE1.9% 1.7%
PAIN1.9% 1.5%
ANAEMIA1.1% 1.9%
DRUG INTERACTION1.9% 1%
MYALGIA1.9% 0.6%
MALAISE1.8% 1.1%
PAIN IN EXTREMITY1.7% 0.8%
NEUTROPENIA0% 1.7%
ARTHRALGIA1.6% 1%
THROMBOCYTOPENIA0.4% 1.6%
RENAL FAILURE ACUTE1% 1.4%
DEATH1.1% 1.3%
OFF LABEL USE1.1% 1.3%
WEIGHT DECREASED1.3% 1.1%
ACUTE KIDNEY INJURY1% 1.3%
PANCYTOPENIA0% 1.3%
RHABDOMYOLYSIS1.3% 0%
HYPOTENSION1.2% 1.2%
PRURITUS1.2% 1.2%
ABDOMINAL PAIN0.9% 1.2%
CONFUSIONAL STATE1.2% 0.9%
RENAL FAILURE0.9% 1.2%
URINARY TRACT INFECTION0.8% 1.2%
CHEST PAIN1.2% 0.8%
INSOMNIA1.2% 0.7%
SEPSIS0.6% 1.2%
COUGH1.1% 1%
DEHYDRATION0.9% 1.1%
GAIT DISTURBANCE1.1% 0.5%
FEBRILE NEUTROPENIA0% 1.1%
DECREASED APPETITE1% 1%
BACK PAIN1% 0.9%
HYPERTENSION1% 0.8%
DEPRESSION1% 0.7%
BLOOD CREATININE INCREASED0.5% 1%
MUSCLE SPASMS1% 0.5%
MUSCULAR WEAKNESS1% 0%
PLATELET COUNT DECREASED0% 1%
BLOOD GLUCOSE INCREASED1% 0%
MYOCARDIAL INFARCTION1% 0%
GASTROINTESTINAL HAEMORRHAGE1% 0%
OEDEMA PERIPHERAL0.9% 0.9%
ANXIETY0.9% 0.9%
CONSTIPATION0.9% 0.8%
HAEMOGLOBIN DECREASED0.6% 0.9%
FLUSHING0.9% 0%
FEELING ABNORMAL0.9% 0%
WHITE BLOOD CELL COUNT DECREASED0% 0.9%
CEREBROVASCULAR ACCIDENT0.9% 0%
CONDITION AGGRAVATED0.8% 0.8%
ABDOMINAL PAIN UPPER0.8% 0.6%
ATRIAL FIBRILLATION0.8% 0.6%
SOMNOLENCE0.8% 0.5%
PARAESTHESIA0.8% 0.5%
SYNCOPE0.8% 0%
DRUG DOSE OMISSION0.8% 0%
CHILLS0% 0.8%
HYPERKALAEMIA0% 0.8%
INFECTION0% 0.8%
ALANINE AMINOTRANSFERASE INCREASED0% 0.8%
PULMONARY EMBOLISM0% 0.8%
TREMOR0.7% 0.7%
ERYTHEMA0.6% 0.7%
WEIGHT INCREASED0.7% 0.5%
LOSS OF CONSCIOUSNESS0.7% 0.5%
HYPOAESTHESIA0.7% 0.5%
HYPERSENSITIVITY0.5% 0.7%
RESPIRATORY FAILURE0% 0.7%
BLOOD PRESSURE INCREASED0.7% 0%
DEEP VEIN THROMBOSIS0% 0.7%
ASPARTATE AMINOTRANSFERASE INCREASED0% 0.7%
LEUKOPENIA0% 0.7%
SEPTIC SHOCK0% 0.7%
HYPERHIDROSIS0.7% 0%
NEUROPATHY PERIPHERAL0% 0.7%
GENERAL PHYSICAL HEALTH DETERIORATION0.6% 0.6%
HYPONATRAEMIA0.5% 0.6%
TACHYCARDIA0% 0.6%
DISEASE PROGRESSION0% 0.6%
PLEURAL EFFUSION0% 0.6%
STEVENS-JOHNSON SYNDROME0% 0.6%
RASH MACULO-PAPULAR0% 0.6%
URTICARIA0% 0.6%
BALANCE DISORDER0.6% 0%
ALOPECIA0.6% 0%
INJECTION SITE PAIN0.6% 0%
MEMORY IMPAIRMENT0.6% 0%
BLOOD CREATINE PHOSPHOKINASE INCREASED0.6% 0%
ABDOMINAL DISCOMFORT0.6% 0%
CARDIAC FAILURE CONGESTIVE0.6% 0%
RENAL IMPAIRMENT0.5% 0.5%
DYSPHAGIA0.4% 0.5%
PRODUCT QUALITY ISSUE0.5% 0%
BRONCHITIS0% 0.5%
SINUSITIS0% 0.5%
CELLULITIS0% 0.5%
CYTOMEGALOVIRUS INFECTION0% 0.5%
AGRANULOCYTOSIS0% 0.5%
HYPOKALAEMIA0% 0.5%
VISION BLURRED0.5% 0%
PALPITATIONS0.5% 0%
CONTUSION0.5% 0%
HEPATOCELLULAR INJURY0% 0.5%
PERIPHERAL SWELLING0.5% 0%
NASOPHARYNGITIS0.5% 0%
DYSPEPSIA0.5% 0%
HYPOGLYCAEMIA0.5% 0%
EPISTAXIS0.5% 0%
DIABETES MELLITUS0.5% 0%
DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS0% 0.5%
CONVULSION0% 0.5%
LUNG DISORDER0% 0.4%
NEUTROPHIL COUNT DECREASED0% 0.4%
CHOLESTASIS0% 0.4%
STAPHYLOCOCCAL INFECTION0% 0.4%
CHRONIC KIDNEY DISEASE0.4% 0%
INTERNATIONAL NORMALISED RATIO INCREASED0.4% 0%
CARDIAC FAILURE0.4% 0%
AMNESIA0.4% 0%
BRADYCARDIA0.4% 0%
INCORRECT DOSE ADMINISTERED0.4% 0%
JOINT SWELLING0.4% 0%
BLOOD ALKALINE PHOSPHATASE INCREASED0% 0.4%

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