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Propranolol and Loratadine

Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side EffectPropranololLoratadine
DRUG INEFFECTIVE2.7% 4.1%
NAUSEA3.1% 3.1%
FATIGUE2.7% 3.1%
DYSPNOEA2.1% 2.9%
HEADACHE2.7% 2.6%
DIZZINESS2.4% 2.6%
DIARRHOEA2.2% 2.4%
PAIN1.7% 2.2%
TOXICITY TO VARIOUS AGENTS2% 0.5%
COMPLETED SUICIDE2% 0%
VOMITING1.9% 1.7%
ANXIETY1.9% 1.4%
OFF LABEL USE1.4% 1.9%
MALAISE1.6% 1.8%
ASTHENIA1.7% 1.6%
DEPRESSION1.7% 1.4%
HYPOTENSION1.7% 0.7%
FALL1.6% 1.5%
INSOMNIA1.6% 1.5%
DRUG INTERACTION1.6% 0.7%
PNEUMONIA0.9% 1.5%
TREMOR1.5% 0.8%
RASH0.8% 1.5%
SOMNOLENCE1.3% 1.4%
ARTHRALGIA1.1% 1.4%
PAIN IN EXTREMITY1.1% 1.4%
COUGH0.9% 1.4%
PYREXIA1.1% 1.3%
CONFUSIONAL STATE1.3% 0.9%
PRURITUS0.8% 1.3%
WEIGHT DECREASED1.2% 1.1%
CHEST PAIN0.9% 1.2%
BACK PAIN0.9% 1.2%
OVERDOSE1.2% 0.5%
BRADYCARDIA1.2% 0%
CARDIAC ARREST1.2% 0%
FEELING ABNORMAL1.1% 1.1%
CONDITION AGGRAVATED1.1% 1.1%
WEIGHT INCREASED1.1% 1%
HYPERTENSION1.1% 1%
ABDOMINAL PAIN1.1% 0.9%
DEATH1% 0.9%
CONSTIPATION0.7% 1%
HYPERHIDROSIS1% 0.7%
SUICIDAL IDEATION1% 0.5%
URTICARIA0% 1%
DECREASED APPETITE0.9% 0.9%
ANAEMIA0.9% 0.7%
PARAESTHESIA0.9% 0.7%
GAIT DISTURBANCE0.9% 0.7%
PALPITATIONS0.9% 0.7%
ABDOMINAL PAIN UPPER0.7% 0.9%
MUSCLE SPASMS0.6% 0.9%
HYPERSENSITIVITY0.5% 0.9%
MIGRAINE0.9% 0%
ASTHMA0% 0.9%
BLOOD PRESSURE INCREASED0.8% 0.7%
DRUG DOSE OMISSION0.7% 0.8%
MEMORY IMPAIRMENT0.8% 0.6%
HYPOAESTHESIA0.6% 0.8%
URINARY TRACT INFECTION0.6% 0.8%
LOSS OF CONSCIOUSNESS0.8% 0.6%
VISION BLURRED0.8% 0.6%
SINUSITIS0% 0.8%
MYALGIA0.7% 0.7%
ALOPECIA0.6% 0.7%
OEDEMA PERIPHERAL0.6% 0.7%
DEHYDRATION0.6% 0.7%
RENAL FAILURE0.6% 0.7%
CHEST DISCOMFORT0.5% 0.7%
AGITATION0.7% 0.5%
ACUTE KIDNEY INJURY0.5% 0.7%
GASTROOESOPHAGEAL REFLUX DISEASE0% 0.7%
NASOPHARYNGITIS0% 0.7%
CHRONIC KIDNEY DISEASE0% 0.7%
CARDIO-RESPIRATORY ARREST0.7% 0%
HEART RATE INCREASED0.6% 0.6%
SYNCOPE0.6% 0.6%
CEREBROVASCULAR ACCIDENT0.5% 0.6%
MUSCULAR WEAKNESS0.6% 0.5%
ABDOMINAL DISCOMFORT0.5% 0.6%
ERYTHEMA0.5% 0.6%
INCORRECT DOSE ADMINISTERED0% 0.6%
DRY MOUTH0% 0.6%
MYOCARDIAL INFARCTION0% 0.6%
DRUG HYPERSENSITIVITY0% 0.6%
INJECTION SITE PAIN0% 0.6%
PERIPHERAL SWELLING0% 0.6%
INTENTIONAL OVERDOSE0.6% 0%
CONVULSION0.6% 0%
HALLUCINATION0.6% 0%
TACHYCARDIA0.6% 0%
HYPOGLYCAEMIA0.6% 0%
BLOOD GLUCOSE INCREASED0.5% 0.5%
CHILLS0.5% 0.5%
PRODUCT USE ISSUE0.5% 0.5%
BALANCE DISORDER0.5% 0.5%
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION0% 0.5%
FLUSHING0% 0.5%
GASTROINTESTINAL HAEMORRHAGE0% 0.5%
ATRIAL FIBRILLATION0% 0.5%
PULMONARY EMBOLISM0% 0.5%
SEPSIS0% 0.5%
HAEMOGLOBIN DECREASED0% 0.5%
EPISTAXIS0% 0.5%
DYSPEPSIA0% 0.5%
BRONCHITIS0% 0.5%
OROPHARYNGEAL PAIN0% 0.5%
EXPIRED PRODUCT ADMINISTERED0% 0.5%
DIABETES MELLITUS0.5% 0%
VISUAL IMPAIRMENT0.5% 0%
WITHDRAWAL SYNDROME0.5% 0%
IRRITABILITY0.5% 0%
RENAL FAILURE ACUTE0.5% 0%
SEIZURE0.5% 0%
ASCITES0.5% 0%
DRUG WITHDRAWAL SYNDROME0.5% 0%
AGGRESSION0.5% 0%
GENERAL PHYSICAL HEALTH DETERIORATION0.5% 0%
SUICIDE ATTEMPT0.5% 0%
COMA0.5% 0%
LETHARGY0.5% 0%
THROMBOCYTOPENIA0.5% 0%
AMNESIA0.5% 0%
SWELLING FACE0% 0.5%

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