Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side Effect Propranolol Baclofen
FALL 1.7% 3.1%
NAUSEA 3% 2.6%
FATIGUE 2.5% 2.9%
PAIN 1.8% 2.9%
DRUG INEFFECTIVE 2.5% 2.8%
HEADACHE 2.6% 2.4%
DIZZINESS 2.4% 2%
GAIT DISTURBANCE 0.9% 2.4%
DYSPNOEA 2.2% 1.4%
MULTIPLE SCLEROSIS RELAPSE 0% 2.2%
ASTHENIA 1.7% 2.1%
DIARRHOEA 2.1% 1.6%
URINARY TRACT INFECTION 0.7% 2.1%
MUSCLE SPASMS 0.7% 2%
VOMITING 1.9% 1.7%
ANXIETY 1.9% 1.2%
INSOMNIA 1.7% 1.6%
MALAISE 1.7% 1.5%
DEPRESSION 1.7% 1.5%
HYPOTENSION 1.7% 0.7%
COMPLETED SUICIDE 1.7% 0.6%
DRUG INTERACTION 1.6% 0.4%
PAIN IN EXTREMITY 1.1% 1.5%
TREMOR 1.4% 1.1%
CONDITION AGGRAVATED 1.1% 1.4%
BACK PAIN 0.9% 1.4%
TOXICITY TO VARIOUS AGENTS 1.4% 0.7%
MUSCULAR WEAKNESS 0.6% 1.4%
MULTIPLE SCLEROSIS 0% 1.4%
SOMNOLENCE 1.3% 1.3%
PYREXIA 1.1% 1.3%
CONFUSIONAL STATE 1.3% 1.1%
MUSCLE SPASTICITY 0% 1.3%
PNEUMONIA 1% 1.2%
OVERDOSE 1.2% 1%
HYPERTENSION 1.2% 0.9%
WEIGHT DECREASED 1.2% 0.9%
HYPOAESTHESIA 0.6% 1.2%
DRUG WITHDRAWAL SYNDROME 0.5% 1.2%
BALANCE DISORDER 0.5% 1.2%
CARDIAC ARREST 1.2% 0%
ARTHRALGIA 1.1% 1.1%
FEELING ABNORMAL 1.1% 1.1%
OFF LABEL USE 1.1% 0.9%
HYPERHIDROSIS 1.1% 0.7%
WEIGHT INCREASED 1.1% 0.7%
ABDOMINAL PAIN 1.1% 0.6%
BRADYCARDIA 1.1% 0%
SUICIDAL IDEATION 1.1% 0%
PARAESTHESIA 0.9% 1%
MEMORY IMPAIRMENT 0.7% 1%
CHEST PAIN 1% 0.7%
CONSTIPATION 0.7% 1%
DRUG DOSE OMISSION 0.6% 1%
ANAEMIA 1% 0.5%
PALPITATIONS 1% 0%
PRURITUS 0.9% 0.9%
CONVULSION 0.8% 0.9%
DEATH 0.9% 0.7%
DECREASED APPETITE 0.9% 0.6%
BLOOD PRESSURE INCREASED 0.9% 0.6%
COUGH 0.9% 0.5%
FLUSHING 0% 0.9%
RASH 0.8% 0.8%
LOSS OF CONSCIOUSNESS 0.8% 0.8%
MIGRAINE 0.8% 0.5%
INFLUENZA LIKE ILLNESS 0% 0.8%
VISION BLURRED 0.7% 0.7%
OEDEMA PERIPHERAL 0.7% 0.6%
ABDOMINAL PAIN UPPER 0.7% 0.6%
MYALGIA 0.7% 0.5%
AGITATION 0.7% 0.4%
MUSCULOSKELETAL STIFFNESS 0% 0.7%
ABASIA 0% 0.7%
DEHYDRATION 0.6% 0.6%
LETHARGY 0.6% 0.4%
HEART RATE INCREASED 0.6% 0.4%
SEIZURE 0% 0.6%
MOBILITY DECREASED 0% 0.6%
DYSPHAGIA 0% 0.6%
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION 0% 0.6%
THERAPY CESSATION 0% 0.6%
COMA 0% 0.6%
HYPOGLYCAEMIA 0.6% 0%
BLOOD GLUCOSE INCREASED 0.6% 0%
AGGRESSION 0.6% 0%
CEREBROVASCULAR ACCIDENT 0.6% 0%
CARDIO-RESPIRATORY ARREST 0.6% 0%
RENAL FAILURE 0.6% 0%
TACHYCARDIA 0.6% 0%
SYNCOPE 0.6% 0%
DIABETES MELLITUS 0.6% 0%
RENAL FAILURE ACUTE 0.6% 0%
ALOPECIA 0.5% 0.5%
SEPSIS 0.5% 0.5%
CHILLS 0.5% 0.5%
HALLUCINATION 0.5% 0.4%
MYOCARDIAL INFARCTION 0.5% 0.4%
ERYTHEMA 0.5% 0.4%
AMNESIA 0.5% 0.4%
VISUAL IMPAIRMENT 0.5% 0.4%
INJECTION SITE PAIN 0.4% 0.5%
INFECTION 0% 0.5%
BURNING SENSATION 0% 0.5%
ABDOMINAL DISCOMFORT 0% 0.5%
MENTAL STATUS CHANGES 0% 0.5%
INJECTION SITE ERYTHEMA 0% 0.5%
CONTUSION 0% 0.5%
RESPIRATORY ARREST 0.5% 0%
INTENTIONAL OVERDOSE 0.5% 0%
ATRIAL FIBRILLATION 0.5% 0%
GENERAL PHYSICAL HEALTH DETERIORATION 0.5% 0%
CHEST DISCOMFORT 0.5% 0%
PULMONARY EMBOLISM 0.5% 0%
SUICIDE ATTEMPT 0.5% 0%
THROMBOCYTOPENIA 0.5% 0%
ASCITES 0.5% 0%
DISORIENTATION 0.5% 0%
IRRITABILITY 0.5% 0%
URINARY INCONTINENCE 0% 0.4%
DRUG HYPERSENSITIVITY 0% 0.4%
NO THERAPEUTIC RESPONSE 0% 0.4%
THERAPEUTIC RESPONSE UNEXPECTED 0% 0.4%
NASOPHARYNGITIS 0% 0.4%
WHITE BLOOD CELL COUNT DECREASED 0% 0.4%

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