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Ritalin and Levitra

Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side EffectRitalinLevitra
ERECTILE DYSFUNCTION0% 16.5%
DRUG INEFFECTIVE4.2% 13.1%
HEADACHE2.9% 7.3%
FLUSHING0% 3.5%
FATIGUE3.4% 1.2%
NAUSEA3% 1.6%
DEPRESSION2.8% 0.6%
ANXIETY2.7% 0.8%
DIZZINESS1.9% 2.4%
ERECTION INCREASED0% 2.4%
NASAL CONGESTION0% 2.3%
FEELING ABNORMAL2.1% 0.8%
INSOMNIA2% 0.7%
SOMNOLENCE2% 0.3%
PAIN1.7% 0.8%
WEIGHT DECREASED1.7% 0.5%
ADVERSE EVENT0% 1.7%
VOMITING1.6% 0.8%
FALL1.6% 0.6%
MALAISE1.5% 0.6%
HYPERTENSION1.4% 1%
DYSPNOEA1.4% 0.9%
ASTHENIA1.4% 0.7%
VISION BLURRED0.6% 1.4%
DECREASED APPETITE1.4% 0%
SUICIDAL IDEATION1.4% 0%
OFF LABEL USE1.4% 0%
DIARRHOEA1.3% 1.1%
TREMOR1.3% 0.3%
WEIGHT INCREASED1.3% 0%
AGITATION1.3% 0%
AGGRESSION1.3% 0%
CONDITION AGGRAVATED1.2% 0.4%
DISTURBANCE IN ATTENTION1.2% 0%
DRUG EFFECT DECREASED0.5% 1.1%
ABNORMAL BEHAVIOUR1.1% 0%
CHEST PAIN0.9% 1%
PAIN IN EXTREMITY1% 0.7%
CONFUSIONAL STATE1% 0%
DRUG DOSE OMISSION1% 0%
DYSPEPSIA0% 1%
MYOCARDIAL INFARCTION0% 1%
BACK PAIN0.9% 0.9%
ARTHRALGIA0.9% 0.6%
HYPERHIDROSIS0.9% 0.5%
GAIT DISTURBANCE0.9% 0.4%
PYREXIA0.9% 0.4%
TACHYCARDIA0.9% 0.3%
BLOOD PRESSURE INCREASED0.9% 0.3%
MEMORY IMPAIRMENT0.9% 0%
HEART RATE INCREASED0.6% 0.8%
RASH0.8% 0.6%
UNEVALUABLE EVENT0.8% 0.5%
ABDOMINAL PAIN UPPER0.8% 0.5%
PARAESTHESIA0.8% 0.5%
MUSCLE SPASMS0.8% 0.4%
HYPOAESTHESIA0.8% 0.3%
ERYTHEMA0% 0.8%
IRRITABILITY0.8% 0%
THERAPEUTIC RESPONSE UNEXPECTED0.8% 0%
PALPITATIONS0.7% 0.6%
DRUG INTERACTION0.7% 0.4%
COUGH0.7% 0.4%
CONSTIPATION0.7% 0.3%
ABDOMINAL PAIN0.7% 0.3%
DEATH0.7% 0.3%
PRE-EXISTING CONDITION IMPROVED0.7% 0%
NASOPHARYNGITIS0.7% 0%
HYPOTENSION0% 0.7%
NO ADVERSE EVENT0% 0.7%
DRUG ABUSE0.7% 0%
SLEEP APNOEA SYNDROME0.7% 0%
PNEUMONIA0.7% 0%
HYPERSENSITIVITY0.7% 0%
SUICIDE ATTEMPT0.7% 0%
OVERDOSE0.7% 0%
HALLUCINATION0.7% 0%
LOSS OF CONSCIOUSNESS0.6% 0.6%
DRUG USE FOR UNKNOWN INDICATION0% 0.6%
CONVULSION0.6% 0%
DRUG DEPENDENCE0.6% 0%
TOXICITY TO VARIOUS AGENTS0.6% 0%
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS0.6% 0%
MIGRAINE0.6% 0%
PRODUCT USE ISSUE0.6% 0%
DEHYDRATION0.6% 0%
FEELING HOT0% 0.6%
TINNITUS0% 0.6%
BLOOD PRESSURE DECREASED0% 0.6%
NO ADVERSE DRUG EFFECT0% 0.6%
VISUAL DISTURBANCE0% 0.6%
ABDOMINAL DISCOMFORT0.5% 0.4%
PRURITUS0.5% 0.3%
INTENTIONAL PRODUCT USE ISSUE0.5% 0%
STRESS0.5% 0%
EJACULATION FAILURE0% 0.5%
MUSCULAR WEAKNESS0.5% 0%
URINARY TRACT INFECTION0.5% 0%
ALOPECIA0.5% 0%
SLEEP DISORDER0.5% 0%
MYALGIA0% 0.5%
BLINDNESS UNILATERAL0% 0.5%
SPONTANEOUS PENILE ERECTION0% 0.5%
PRIAPISM0% 0.5%
VISUAL IMPAIRMENT0% 0.5%
CRYING0.5% 0%
VISUAL ACUITY REDUCED0% 0.5%
CEREBROVASCULAR ACCIDENT0% 0.5%
SINUSITIS0.5% 0%
EJACULATION DISORDER0% 0.5%
SEIZURE0.5% 0%
DRUG HYPERSENSITIVITY0.5% 0%
PSYCHOMOTOR HYPERACTIVITY0.5% 0%
DRY MOUTH0.5% 0%
DEPRESSED MOOD0.5% 0%
DRUG WITHDRAWAL SYNDROME0.5% 0%
NERVOUSNESS0.5% 0%
PSYCHOTIC DISORDER0.5% 0%
PRODUCT QUALITY ISSUE0.5% 0%
ANGER0.5% 0%
AMNESIA0.5% 0%
DYSKINESIA0.5% 0%
BALANCE DISORDER0.5% 0%
OEDEMA PERIPHERAL0.4% 0.3%
RHINORRHOEA0% 0.4%
BLOOD CHOLESTEROL INCREASED0% 0.4%
PENIS DISORDER0% 0.4%
GASTROOESOPHAGEAL REFLUX DISEASE0% 0.4%
CHEST DISCOMFORT0% 0.4%
DIABETES MELLITUS0% 0.4%
CORONARY ARTERY DISEASE0% 0.4%
ATRIAL FIBRILLATION0% 0.4%
BLOOD GLUCOSE INCREASED0% 0.4%
INCORRECT DOSE ADMINISTERED0.4% 0%
BLINDNESS0% 0.4%
CYANOPSIA0% 0.4%
CARDIAC FAILURE CONGESTIVE0% 0.4%
OPTIC ISCHAEMIC NEUROPATHY0% 0.4%
OCULAR HYPERAEMIA0% 0.4%
SYNCOPE0% 0.4%
ANAEMIA0% 0.3%
DEAFNESS0% 0.3%
PULMONARY EMBOLISM0% 0.3%
EYE PAIN0% 0.3%
DYSURIA0% 0.3%
PENILE PAIN0% 0.3%
BLINDNESS TRANSIENT0% 0.3%
ANORGASMIA0% 0.3%
CHILLS0% 0.3%
STOMACH DISCOMFORT0% 0.3%
THERAPEUTIC RESPONSE DELAYED0% 0.3%

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