Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side Effect Hyzaar Propafenone
ATRIAL FIBRILLATION 0.8% 4.9%
DRUG INEFFECTIVE 2.9% 3.5%
NAUSEA 3.3% 2.9%
DIZZINESS 2.6% 3.2%
DYSPNOEA 2.3% 2.7%
TOXICITY TO VARIOUS AGENTS 0% 2.6%
FATIGUE 2.5% 2.3%
HEADACHE 2.4% 1.6%
CARDIAC ARREST 0% 2.3%
DIARRHOEA 2.2% 1.6%
PAIN 2.1% 1.1%
DRUG INTERACTION 0.7% 2.1%
ASTHENIA 2% 1.9%
FALL 1.6% 2%
VOMITING 1.8% 1.6%
MYOCARDIAL INFARCTION 1.8% 0.9%
COMPLETED SUICIDE 0% 1.8%
HYPOTENSION 1% 1.7%
ARTHRALGIA 1.7% 1%
HYPERTENSION 1.7% 0.8%
ARRHYTHMIA 0% 1.7%
BLOOD GLUCOSE INCREASED 1.6% 0%
MALAISE 1.5% 1.5%
BLOOD PRESSURE INCREASED 1.5% 1.2%
GASTROINTESTINAL HAEMORRHAGE 0.5% 1.5%
CHEST PAIN 1.4% 1.2%
PAIN IN EXTREMITY 1.4% 0.9%
PALPITATIONS 0.8% 1.4%
PRURITUS 1.4% 0.7%
WEIGHT DECREASED 1.4% 0.7%
COUGH 1.4% 0.4%
CEREBROVASCULAR ACCIDENT 1.3% 0.8%
ANXIETY 1.3% 0.8%
OEDEMA PERIPHERAL 1.3% 0.7%
RASH 1.2% 0.8%
INSOMNIA 1.2% 0.7%
BACK PAIN 1.2% 0.6%
CARDIAC FAILURE CONGESTIVE 1.2% 0.5%
SOMNOLENCE 0.9% 1.1%
RENAL FAILURE ACUTE 1.1% 0.7%
SYNCOPE 0.7% 1.1%
PRODUCT QUALITY ISSUE 0.5% 1.1%
DEHYDRATION 1.1% 0.5%
MYALGIA 1.1% 0.5%
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED 0% 1.1%
DEPRESSION 1.1% 0%
WEIGHT INCREASED 1.1% 0%
ANAEMIA 1% 1%
FEELING ABNORMAL 0.9% 1%
CONSTIPATION 0.9% 1%
PNEUMONIA 1% 0.7%
HEART RATE INCREASED 0.5% 1%
RENAL FAILURE 1% 0%
MUSCLE SPASMS 1% 0%
FLUSHING 1% 0%
OVERDOSE 0% 1%
LOSS OF CONSCIOUSNESS 0.9% 0.9%
ABDOMINAL PAIN 0.8% 0.9%
PYREXIA 0.9% 0.7%
BRADYCARDIA 0% 0.9%
INTERNATIONAL NORMALISED RATIO INCREASED 0% 0.9%
CORONARY ARTERY DISEASE 0.9% 0%
HYPONATRAEMIA 0.9% 0%
URINARY TRACT INFECTION 0.7% 0.8%
HYPERHIDROSIS 0.8% 0.7%
DYSPEPSIA 0.6% 0.8%
DEATH 0.6% 0.8%
DECREASED APPETITE 0.8% 0.6%
TREMOR 0.8% 0.6%
HAEMOGLOBIN DECREASED 0.5% 0.8%
HYPOAESTHESIA 0.8% 0.4%
GAIT DISTURBANCE 0.8% 0.4%
OFF LABEL USE 0% 0.8%
HYPOKALAEMIA 0.8% 0%
TACHYCARDIA 0% 0.8%
ERYTHEMA 0.7% 0.7%
ABDOMINAL PAIN UPPER 0.6% 0.7%
VISION BLURRED 0.7% 0.5%
CONFUSIONAL STATE 0.7% 0.5%
CONTUSION 0% 0.7%
MUSCULAR WEAKNESS 0.7% 0%
DRUG DOSE OMISSION 0% 0.7%
ACUTE KIDNEY INJURY 0% 0.7%
DIABETES MELLITUS 0.7% 0%
SUICIDE ATTEMPT 0% 0.7%
PARAESTHESIA 0.7% 0%
BLOOD PRESSURE DECREASED 0.5% 0.6%
CONDITION AGGRAVATED 0.6% 0.5%
BALANCE DISORDER 0.5% 0.6%
CHEST DISCOMFORT 0.4% 0.6%
TRANSIENT ISCHAEMIC ATTACK 0.6% 0.4%
ALOPECIA 0.6% 0%
INJURY 0.6% 0%
BLOOD CHOLESTEROL INCREASED 0.6% 0%
HEART RATE IRREGULAR 0% 0.6%
MEMORY IMPAIRMENT 0% 0.6%
ABDOMINAL DISCOMFORT 0% 0.6%
PRODUCT SUBSTITUTION ISSUE 0% 0.6%
GASTROOESOPHAGEAL REFLUX DISEASE 0.6% 0%
INJECTION SITE PAIN 0.6% 0%
RECTAL HAEMORRHAGE 0% 0.6%
BLOOD CREATININE INCREASED 0.6% 0%
OSTEOARTHRITIS 0.6% 0%
NASOPHARYNGITIS 0.6% 0%
JOINT SWELLING 0.5% 0.4%
DRY MOUTH 0.5% 0.4%
DYSGEUSIA 0.4% 0.5%
EPISTAXIS 0% 0.5%
CARDIAC FAILURE 0% 0.5%
CARDIO-RESPIRATORY ARREST 0% 0.5%
HAEMATURIA 0% 0.5%
HAEMORRHAGE 0% 0.5%
ELECTROCARDIOGRAM QT PROLONGED 0% 0.5%
INTENTIONAL OVERDOSE 0% 0.5%
SUPRAVENTRICULAR TACHYCARDIA 0% 0.5%
URTICARIA 0.5% 0%
VENTRICULAR TACHYCARDIA 0% 0.5%
ARTHRITIS 0.5% 0%
PULMONARY EMBOLISM 0.5% 0%
DYSPHAGIA 0.5% 0%
CONVULSION 0% 0.5%
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION 0% 0.5%
PANCREATITIS 0.5% 0%
HYPERSENSITIVITY 0.5% 0%
CARDIAC DISORDER 0.5% 0%
BLOOD POTASSIUM DECREASED 0.5% 0%
SINUSITIS 0.5% 0%
VENTRICULAR FIBRILLATION 0% 0.4%
LOWER GASTROINTESTINAL HAEMORRHAGE 0% 0.4%
CHILLS 0.4% 0%
ACUTE MYOCARDIAL INFARCTION 0.4% 0%
RHABDOMYOLYSIS 0.4% 0%

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