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Concerta and Lipitor

Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side EffectConcertaLipitor
DRUG INEFFECTIVE5.3% 2.8%
TYPE 2 DIABETES MELLITUS0% 3.7%
HEADACHE2.9% 1.9%
NAUSEA2.4% 2.7%
FATIGUE2.2% 2.7%
MYALGIA0% 2.7%
INSOMNIA2.3% 1.2%
ANXIETY2.3% 1.1%
DEPRESSION2.3% 1.1%
DYSPNOEA1% 2.3%
DIZZINESS1.6% 2.2%
PAIN1.1% 2.1%
DIARRHOEA0.8% 2.1%
AGGRESSION2.1% 0%
OFF LABEL USE2% 0.8%
ASTHENIA0.7% 2%
PAIN IN EXTREMITY0.5% 2%
MYOCARDIAL INFARCTION0% 2%
SUICIDAL IDEATION2% 0%
DRUG DOSE OMISSION1.9% 0.6%
DECREASED APPETITE1.8% 0.9%
ARTHRALGIA0.5% 1.8%
ABNORMAL BEHAVIOUR1.8% 0%
VOMITING1.7% 1.4%
DISTURBANCE IN ATTENTION1.7% 0%
WEIGHT DECREASED1.6% 1.4%
FEELING ABNORMAL1.6% 0.9%
FALL0.6% 1.6%
MALAISE1.1% 1.5%
WEIGHT INCREASED1.5% 1%
SOMNOLENCE1.5% 0.7%
MUSCLE SPASMS0.5% 1.5%
AGITATION1.5% 0%
DRUG HYPERSENSITIVITY0% 1.5%
DEATH0% 1.4%
HYPERTENSION1.2% 1.3%
CHEST PAIN0.9% 1.3%
CEREBROVASCULAR ACCIDENT0% 1.3%
PRODUCT SUBSTITUTION ISSUE1.3% 0%
BACK PAIN0.5% 1.2%
TACHYCARDIA1.2% 0%
IRRITABILITY1.2% 0%
BLOOD GLUCOSE INCREASED0% 1.2%
SUICIDE ATTEMPT1.2% 0%
RASH0.8% 1.1%
PRURITUS0.7% 1.1%
TREMOR1.1% 0.6%
MUSCULAR WEAKNESS0% 1.1%
PNEUMONIA0% 1.1%
COUGH0.5% 1%
CONSTIPATION0.4% 1%
GAIT DISTURBANCE0% 1%
HALLUCINATION1% 0%
OVERDOSE1% 0%
DRUG EFFECT DECREASED1% 0%
PRODUCT USE ISSUE1% 0%
OEDEMA PERIPHERAL0% 1%
PYREXIA0.8% 0.9%
DRUG INTERACTION0.9% 0.7%
CONDITION AGGRAVATED0.9% 0.7%
PALPITATIONS0.9% 0.5%
RENAL FAILURE0% 0.9%
BLOOD CHOLESTEROL INCREASED0% 0.9%
CARDIAC FAILURE CONGESTIVE0% 0.9%
PSYCHOTIC DISORDER0.9% 0%
HEART RATE INCREASED0.9% 0%
TIC0.9% 0%
ANAEMIA0% 0.9%
ABDOMINAL PAIN UPPER0.8% 0.8%
ABDOMINAL PAIN0.8% 0.8%
BLOOD PRESSURE INCREASED0.7% 0.8%
GYNAECOMASTIA0.8% 0%
HYPOTENSION0% 0.8%
DIABETES MELLITUS0% 0.8%
FLUSHING0% 0.8%
ANGER0.8% 0%
PSYCHOMOTOR HYPERACTIVITY0.8% 0%
TOXICITY TO VARIOUS AGENTS0.8% 0%
CONFUSIONAL STATE0.7% 0.7%
HYPERHIDROSIS0.7% 0.6%
HYPOAESTHESIA0.5% 0.7%
PARAESTHESIA0.5% 0.7%
HOSPITALISATION0.7% 0%
INCORRECT DOSE ADMINISTERED0.7% 0%
ADVERSE EVENT0.7% 0%
GROWTH RETARDATION0.7% 0%
URINARY TRACT INFECTION0% 0.7%
DEHYDRATION0% 0.7%
ATRIAL FIBRILLATION0% 0.7%
DYSKINESIA0.7% 0%
VISION BLURRED0.6% 0.5%
SYNCOPE0.6% 0.5%
MEMORY IMPAIRMENT0.5% 0.6%
LOSS OF CONSCIOUSNESS0.6% 0.5%
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION0.6% 0%
SLEEP DISORDER0.6% 0%
TREATMENT NONCOMPLIANCE0.6% 0%
CONVULSION0.6% 0%
RESTLESSNESS0.6% 0%
DRUG ABUSE0.6% 0%
MOOD SWINGS0.6% 0%
CARDIAC DISORDER0% 0.6%
CRYING0.6% 0%
PRODUCT QUALITY ISSUE0.6% 0%
GASTROINTESTINAL HAEMORRHAGE0% 0.6%
ABDOMINAL DISCOMFORT0% 0.6%
RHABDOMYOLYSIS0% 0.6%
AMNESIA0% 0.6%
RENAL FAILURE ACUTE0% 0.6%
BLOOD CREATINE PHOSPHOKINASE INCREASED0% 0.6%
CORONARY ARTERY DISEASE0% 0.6%
ALOPECIA0% 0.6%
NASOPHARYNGITIS0.4% 0.5%
HYPERSENSITIVITY0.4% 0.5%
BALANCE DISORDER0% 0.5%
ARTHRITIS0% 0.5%
CONTUSION0% 0.5%
GASTROOESOPHAGEAL REFLUX DISEASE0% 0.5%
HAEMOGLOBIN DECREASED0% 0.5%
DYSPEPSIA0% 0.5%
ERYTHEMA0% 0.5%
NEUROPATHY PERIPHERAL0% 0.5%
DYSPHAGIA0% 0.5%
HALLUCINATION, VISUAL0.5% 0%
ATTENTION DEFICIT/HYPERACTIVITY DISORDER0.5% 0%
HALLUCINATION, AUDITORY0.5% 0%
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS0.5% 0%
EMOTIONAL DISORDER0.5% 0%
INTENTIONAL OVERDOSE0.5% 0%
DEPRESSED MOOD0.5% 0%
MIGRAINE0.5% 0%
COMPLETED SUICIDE0.5% 0%
MUSCULOSKELETAL PAIN0% 0.4%
ASPARTATE AMINOTRANSFERASE INCREASED0% 0.4%
JOINT SWELLING0% 0.4%
CATARACT0% 0.4%
RENAL IMPAIRMENT0% 0.4%
URTICARIA0% 0.4%
DYSGEUSIA0% 0.4%
ALANINE AMINOTRANSFERASE INCREASED0% 0.4%
MOOD ALTERED0.4% 0%
BLOOD CREATININE INCREASED0% 0.4%
CHEST DISCOMFORT0% 0.4%
SPEECH DISORDER0.4% 0%
DYSTONIA0.4% 0%
PRODUCT USE IN UNAPPROVED INDICATION0.4% 0%
UNEVALUABLE EVENT0.4% 0%
DRY MOUTH0.4% 0%
NERVOUSNESS0.4% 0%
INJECTION SITE PAIN0% 0.4%

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