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Augmentin and Propranolol

Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side EffectAugmentinPropranolol
DRUG HYPERSENSITIVITY4% 0%
DIARRHOEA3.5% 2.2%
NAUSEA2.7% 3.1%
PYREXIA3% 1.1%
FATIGUE2.3% 2.7%
DYSPNOEA2.7% 2.1%
HEADACHE1.6% 2.7%
DRUG INEFFECTIVE1.6% 2.7%
DIZZINESS1.3% 2.4%
VOMITING2.3% 1.9%
RASH2.2% 0.8%
PNEUMONIA2% 0.9%
COMPLETED SUICIDE0% 2%
TOXICITY TO VARIOUS AGENTS0% 2%
PAIN1.9% 1.7%
ANXIETY1.2% 1.9%
PRURITUS1.9% 0.8%
ASTHENIA1.7% 1.7%
HYPOTENSION1.3% 1.7%
DEPRESSION0.8% 1.7%
MALAISE1.5% 1.6%
DRUG INTERACTION1.2% 1.6%
FALL1% 1.6%
ANAEMIA1.6% 0.9%
INSOMNIA0.8% 1.6%
TREMOR0% 1.5%
OFF LABEL USE0.8% 1.4%
ABDOMINAL PAIN1.3% 1.1%
CONFUSIONAL STATE0.9% 1.3%
SOMNOLENCE0.6% 1.3%
ERYTHEMA1.3% 0.5%
SINUSITIS1.3% 0%
WEIGHT DECREASED1.1% 1.2%
COUGH1.2% 0.9%
CARDIAC ARREST0.5% 1.2%
OVERDOSE0.5% 1.2%
ACUTE KIDNEY INJURY1.2% 0.5%
BRADYCARDIA0% 1.2%
ARTHRALGIA1% 1.1%
PAIN IN EXTREMITY0.9% 1.1%
CONDITION AGGRAVATED0.8% 1.1%
HYPERTENSION0.8% 1.1%
THROMBOCYTOPENIA1.1% 0.5%
FEELING ABNORMAL0.5% 1.1%
WEIGHT INCREASED0% 1.1%
DEATH1% 1%
DEHYDRATION1% 0.6%
RENAL FAILURE ACUTE1% 0.5%
HYPERHIDROSIS0.5% 1%
URTICARIA1% 0%
SUICIDAL IDEATION0% 1%
CHOLESTASIS1% 0%
DECREASED APPETITE0.9% 0.9%
CHEST PAIN0.9% 0.9%
BACK PAIN0.9% 0.9%
ABDOMINAL PAIN UPPER0.9% 0.7%
URINARY TRACT INFECTION0.9% 0.6%
OEDEMA PERIPHERAL0.9% 0.6%
RENAL FAILURE0.9% 0.6%
PARAESTHESIA0.5% 0.9%
GAIT DISTURBANCE0.5% 0.9%
PALPITATIONS0% 0.9%
HEPATOCELLULAR INJURY0.9% 0%
MIGRAINE0% 0.9%
NEUTROPENIA0.9% 0%
CONSTIPATION0.8% 0.7%
GENERAL PHYSICAL HEALTH DETERIORATION0.8% 0.5%
LOSS OF CONSCIOUSNESS0.5% 0.8%
HYPERSENSITIVITY0.8% 0.5%
BRONCHITIS0.8% 0%
BLOOD PRESSURE INCREASED0% 0.8%
SEPSIS0.8% 0%
VISION BLURRED0% 0.8%
MEMORY IMPAIRMENT0% 0.8%
RASH MACULO-PAPULAR0.8% 0%
JAUNDICE0.8% 0%
PULMONARY EMBOLISM0.8% 0%
MYALGIA0.6% 0.7%
CHILLS0.7% 0.5%
CARDIO-RESPIRATORY ARREST0% 0.7%
AGITATION0% 0.7%
INJURY0.7% 0%
ATRIAL FIBRILLATION0.7% 0%
DEEP VEIN THROMBOSIS0.7% 0%
PANCYTOPENIA0.7% 0%
DRUG DOSE OMISSION0% 0.7%
TACHYCARDIA0.5% 0.6%
HYPOAESTHESIA0.5% 0.6%
MUSCLE SPASMS0.5% 0.6%
MUSCULAR WEAKNESS0% 0.6%
ALOPECIA0% 0.6%
HYPOGLYCAEMIA0% 0.6%
HALLUCINATION0% 0.6%
SYNCOPE0% 0.6%
CONVULSION0% 0.6%
INTENTIONAL OVERDOSE0% 0.6%
HEART RATE INCREASED0% 0.6%
ASPARTATE AMINOTRANSFERASE INCREASED0.6% 0%
CELLULITIS0.6% 0%
HEPATITIS0.6% 0%
DRUG REACTION WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS0.6% 0%
NEUROPATHY PERIPHERAL0.6% 0%
INFECTION0.6% 0%
INTERNATIONAL NORMALISED RATIO INCREASED0.6% 0%
RESPIRATORY FAILURE0.6% 0%
ALANINE AMINOTRANSFERASE INCREASED0.6% 0%
ASCITES0% 0.5%
DIABETES MELLITUS0% 0.5%
DRUG WITHDRAWAL SYNDROME0% 0.5%
ABDOMINAL DISCOMFORT0% 0.5%
CEREBROVASCULAR ACCIDENT0% 0.5%
BLOOD GLUCOSE INCREASED0% 0.5%
SUICIDE ATTEMPT0% 0.5%
COMA0% 0.5%
CHEST DISCOMFORT0% 0.5%
BALANCE DISORDER0% 0.5%
PRODUCT USE ISSUE0% 0.5%
SEIZURE0% 0.5%
IRRITABILITY0% 0.5%
LETHARGY0% 0.5%
WITHDRAWAL SYNDROME0% 0.5%
AGGRESSION0% 0.5%
AGRANULOCYTOSIS0.5% 0%
AMNESIA0% 0.5%
HEPATITIS CHOLESTATIC0.5% 0%
EMOTIONAL DISTRESS0.5% 0%
BLOOD ALKALINE PHOSPHATASE INCREASED0.5% 0%
EOSINOPHILIA0.5% 0%
DYSPHAGIA0.5% 0%
CARDIAC FAILURE0.5% 0%
EPISTAXIS0.5% 0%
UPPER RESPIRATORY TRACT INFECTION0.5% 0%
TOXIC EPIDERMAL NECROLYSIS0.5% 0%
TOXIC SKIN ERUPTION0.5% 0%
LEUKOPENIA0.5% 0%
FEBRILE NEUTROPENIA0.5% 0%
PLEURAL EFFUSION0.5% 0%
ANAPHYLACTIC REACTION0.5% 0%
HAEMOGLOBIN DECREASED0.5% 0%
VISUAL IMPAIRMENT0% 0.5%

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