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Lorazepam and Voltaren

Compare Side Effects

% of total side effects reported by users. DISCLAIMER: ALL DATA PROVIDED AS-IS. Data Source: openfda.gov.
Side EffectLorazepamVoltaren
NAUSEA3.4% 2.6%
DRUG INEFFECTIVE2.6% 3%
FATIGUE3% 2%
DRUG ADMINISTERED AT INAPPROPRIATE SITE0% 3%
PAIN1.9% 2.6%
DIARRHOEA2.5% 2.1%
OFF LABEL USE1.2% 2.5%
DYSPNOEA2.4% 2.1%
VOMITING2.2% 1.9%
ANXIETY2.1% 0.8%
HEADACHE2% 1.8%
DIZZINESS2% 1.7%
ARTHRALGIA1% 2%
PRODUCT USE ISSUE0% 2%
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION0% 2%
FALL1.9% 1.5%
PYREXIA1.5% 1.8%
MALAISE1.4% 1.8%
ASTHENIA1.8% 1.3%
DRUG INTERACTION1.7% 1.1%
PAIN IN EXTREMITY1% 1.7%
INSOMNIA1.6% 0.9%
DEPRESSION1.6% 0.8%
DEATH1.6% 0.7%
COMPLETED SUICIDE1.6% 0%
PNEUMONIA1.5% 1.1%
SOMNOLENCE1.5% 0.8%
RASH1.1% 1.4%
THERAPEUTIC RESPONSE UNEXPECTED0% 1.4%
ANAEMIA1% 1.3%
BACK PAIN1% 1.3%
HYPOTENSION1.3% 0.8%
CONFUSIONAL STATE1.3% 0.6%
WEIGHT DECREASED1.2% 1%
CONDITION AGGRAVATED1% 1.2%
PRURITUS0.8% 1.2%
CONSTIPATION1.2% 0.7%
TOXICITY TO VARIOUS AGENTS1.2% 0%
WRONG TECHNIQUE IN PRODUCT USAGE PROCESS0% 1.2%
TREMOR1.1% 0.6%
RENAL FAILURE ACUTE0.5% 1.1%
OVERDOSE1.1% 0%
ABDOMINAL PAIN1% 1%
HYPERTENSION1% 0.9%
DECREASED APPETITE1% 0.9%
FEELING ABNORMAL1% 0.8%
ABDOMINAL PAIN UPPER0.8% 1%
DEHYDRATION1% 0.7%
HAEMOGLOBIN DECREASED0.6% 1%
WEIGHT INCREASED1% 0.6%
DRUG HYPERSENSITIVITY0% 1%
INCORRECT DOSE ADMINISTERED0% 1%
AGITATION1% 0%
CHEST PAIN0.9% 0.9%
GAIT DISTURBANCE0.9% 0.8%
OEDEMA PERIPHERAL0.7% 0.9%
ERYTHEMA0% 0.9%
SUICIDE ATTEMPT0.9% 0%
RHEUMATOID ARTHRITIS0% 0.9%
DRUG ABUSE0.9% 0%
COUGH0.8% 0.8%
LOSS OF CONSCIOUSNESS0.8% 0.7%
HYPOAESTHESIA0.6% 0.8%
URINARY TRACT INFECTION0.8% 0.6%
TACHYCARDIA0.8% 0%
PARAESTHESIA0.7% 0.7%
MUSCLE SPASMS0.7% 0.7%
RENAL FAILURE0.6% 0.7%
MYALGIA0.6% 0.7%
BLOOD PRESSURE INCREASED0.6% 0.7%
HYPERHIDROSIS0.7% 0.5%
HYPERSENSITIVITY0% 0.7%
ALANINE AMINOTRANSFERASE INCREASED0% 0.7%
BLOOD CREATININE INCREASED0% 0.7%
SUICIDAL IDEATION0.7% 0%
ASPARTATE AMINOTRANSFERASE INCREASED0% 0.7%
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION0% 0.7%
GASTROINTESTINAL HAEMORRHAGE0% 0.7%
SEPSIS0.6% 0.6%
MYOCARDIAL INFARCTION0.6% 0.6%
ABDOMINAL DISCOMFORT0.5% 0.6%
PLATELET COUNT DECREASED0.5% 0.6%
INTENTIONAL OVERDOSE0.6% 0%
SOPOR0.6% 0%
DRUG DOSE OMISSION0.6% 0%
PULMONARY EMBOLISM0.6% 0%
DYSPHAGIA0.6% 0%
OSTEOARTHRITIS0% 0.6%
PERIPHERAL SWELLING0% 0.6%
C-REACTIVE PROTEIN INCREASED0% 0.6%
NASOPHARYNGITIS0% 0.6%
ARTHRITIS0% 0.6%
CONVULSION0.6% 0%
JOINT SWELLING0% 0.6%
URTICARIA0% 0.6%
PRODUCT USE IN UNAPPROVED INDICATION0% 0.6%
NEUTROPENIA0.6% 0%
RESPIRATORY FAILURE0.6% 0%
SYNCOPE0.6% 0%
MEMORY IMPAIRMENT0.6% 0%
ALOPECIA0.6% 0%
HYPONATRAEMIA0.6% 0%
CARDIAC ARREST0.6% 0%
THROMBOCYTOPENIA0.6% 0%
COMA0.6% 0%
GENERAL PHYSICAL HEALTH DETERIORATION0.5% 0.5%
MUSCULAR WEAKNESS0.5% 0.5%
WHITE BLOOD CELL COUNT DECREASED0.5% 0.5%
CHILLS0.5% 0.4%
MUSCULOSKELETAL PAIN0% 0.5%
RENAL IMPAIRMENT0% 0.5%
CARDIO-RESPIRATORY ARREST0.5% 0%
INJECTION SITE PAIN0% 0.5%
MELAENA0% 0.5%
INTERSTITIAL LUNG DISEASE0% 0.5%
INFECTION0% 0.5%
GASTRIC ULCER0% 0.5%
ACUTE KIDNEY INJURY0% 0.5%
HALLUCINATION0.5% 0%
PRODUCT QUALITY ISSUE0% 0.5%
BLOOD PRESSURE DECREASED0% 0.5%
CONTUSION0.5% 0%
CEREBROVASCULAR ACCIDENT0.5% 0%
PALPITATIONS0.5% 0%
AGGRESSION0.5% 0%
NEUROLEPTIC MALIGNANT SYNDROME0.5% 0%
DRUG WITHDRAWAL SYNDROME0.5% 0%
ATRIAL FIBRILLATION0.5% 0%
DIABETES MELLITUS0.5% 0%
HEART RATE INCREASED0.5% 0%
PLEURAL EFFUSION0.5% 0%
DELIRIUM0.5% 0%
VISION BLURRED0.5% 0%
SWELLING0% 0.4%
HEPATIC FUNCTION ABNORMAL0% 0.4%
BLOOD UREA INCREASED0% 0.4%
EXPIRED PRODUCT ADMINISTERED0% 0.4%

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