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Propranolol and Baclofen

Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side EffectPropranololBaclofen
FALL1.6% 3.2%
FATIGUE2.7% 3.1%
NAUSEA3.1% 2.5%
PAIN1.7% 3.1%
DRUG INEFFECTIVE2.7% 2.8%
HEADACHE2.7% 2.3%
DIZZINESS2.4% 2%
GAIT DISTURBANCE0.9% 2.4%
DIARRHOEA2.2% 1.6%
DYSPNOEA2.1% 1.3%
MULTIPLE SCLEROSIS RELAPSE0% 2.1%
ASTHENIA1.7% 2%
TOXICITY TO VARIOUS AGENTS2% 0.8%
COMPLETED SUICIDE2% 0.7%
URINARY TRACT INFECTION0.6% 2%
MUSCLE SPASMS0.6% 2%
VOMITING1.9% 1.6%
ANXIETY1.9% 1.1%
DEPRESSION1.7% 1.5%
HYPOTENSION1.7% 0.7%
INSOMNIA1.6% 1.5%
MALAISE1.6% 1.5%
DRUG INTERACTION1.6% 0.4%
PAIN IN EXTREMITY1.1% 1.5%
CONDITION AGGRAVATED1.1% 1.5%
TREMOR1.5% 1.1%
MUSCLE SPASTICITY0% 1.5%
SOMNOLENCE1.3% 1.4%
OFF LABEL USE1.4% 1.2%
BACK PAIN0.9% 1.4%
MUSCULAR WEAKNESS0.6% 1.4%
DRUG WITHDRAWAL SYNDROME0.5% 1.4%
CONFUSIONAL STATE1.3% 1.1%
HYPOAESTHESIA0.6% 1.3%
MULTIPLE SCLEROSIS0% 1.3%
OVERDOSE1.2% 1.1%
PYREXIA1.1% 1.2%
WEIGHT DECREASED1.2% 0.9%
BALANCE DISORDER0.5% 1.2%
BRADYCARDIA1.2% 0%
CARDIAC ARREST1.2% 0%
FEELING ABNORMAL1.1% 1%
ARTHRALGIA1.1% 1%
PNEUMONIA0.9% 1.1%
HYPERTENSION1.1% 0.8%
MEMORY IMPAIRMENT0.8% 1.1%
WEIGHT INCREASED1.1% 0.6%
ABDOMINAL PAIN1.1% 0.6%
PARAESTHESIA0.9% 1%
DEATH1% 0.8%
DRUG DOSE OMISSION0.7% 1%
HYPERHIDROSIS1% 0.7%
SUICIDAL IDEATION1% 0%
PRURITUS0.8% 0.9%
CHEST PAIN0.9% 0.7%
CONSTIPATION0.7% 0.9%
DECREASED APPETITE0.9% 0.6%
COUGH0.9% 0.5%
MIGRAINE0.9% 0.5%
ANAEMIA0.9% 0.4%
FLUSHING0% 0.9%
PALPITATIONS0.9% 0%
LOSS OF CONSCIOUSNESS0.8% 0.8%
RASH0.8% 0.8%
VISION BLURRED0.8% 0.6%
BLOOD PRESSURE INCREASED0.8% 0.5%
MUSCULOSKELETAL STIFFNESS0% 0.8%
CONVULSION0.6% 0.7%
ABDOMINAL PAIN UPPER0.7% 0.6%
MYALGIA0.7% 0.5%
SEIZURE0.5% 0.7%
MOBILITY DECREASED0% 0.7%
THERAPY CESSATION0% 0.7%
AGITATION0.7% 0%
CARDIO-RESPIRATORY ARREST0.7% 0%
INFLUENZA LIKE ILLNESS0% 0.7%
ALOPECIA0.6% 0.6%
OEDEMA PERIPHERAL0.6% 0.5%
DEHYDRATION0.6% 0.5%
COMA0.5% 0.6%
HALLUCINATION0.6% 0.4%
INTENTIONAL OVERDOSE0.6% 0%
RENAL FAILURE0.6% 0%
SYNCOPE0.6% 0%
TACHYCARDIA0.6% 0%
HYPOGLYCAEMIA0.6% 0%
HEART RATE INCREASED0.6% 0%
ABDOMINAL DISCOMFORT0.5% 0.5%
CHILLS0.5% 0.5%
LETHARGY0.5% 0.4%
ERYTHEMA0.5% 0.4%
AMNESIA0.5% 0.4%
VISUAL IMPAIRMENT0.5% 0.4%
HYPERSENSITIVITY0.5% 0.4%
PERIPHERAL SWELLING0% 0.5%
INJECTION SITE PAIN0% 0.5%
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION0% 0.5%
DRUG HYPERSENSITIVITY0% 0.5%
CONTUSION0% 0.5%
DYSPHAGIA0% 0.5%
BURNING SENSATION0% 0.5%
SEPSIS0% 0.5%
MENTAL STATUS CHANGES0% 0.5%
INFECTION0% 0.5%
ABASIA0% 0.5%
NASOPHARYNGITIS0% 0.5%
IRRITABILITY0.5% 0%
WITHDRAWAL SYNDROME0.5% 0%
BLOOD GLUCOSE INCREASED0.5% 0%
ACUTE KIDNEY INJURY0.5% 0%
THROMBOCYTOPENIA0.5% 0%
CEREBROVASCULAR ACCIDENT0.5% 0%
RENAL FAILURE ACUTE0.5% 0%
SUICIDE ATTEMPT0.5% 0%
GENERAL PHYSICAL HEALTH DETERIORATION0.5% 0%
AGGRESSION0.5% 0%
DIABETES MELLITUS0.5% 0%
ASCITES0.5% 0%
CHEST DISCOMFORT0.5% 0%
PRODUCT USE ISSUE0.5% 0%
WHITE BLOOD CELL COUNT DECREASED0% 0.4%
NO THERAPEUTIC RESPONSE0% 0.4%
THERAPEUTIC RESPONSE UNEXPECTED0% 0.4%
INJECTION SITE ERYTHEMA0% 0.4%
URINARY INCONTINENCE0% 0.4%
UNEVALUABLE EVENT0% 0.4%

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