Please choose an event type to view the corresponding MedsFacts report:

HYPOTHYROIDISM ( 9 FDA reports)
PERICARDIAL EFFUSION ( 9 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
CELLULITIS ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
PAIN ( 3 FDA reports)
RHEUMATOID NODULE ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERKERATOSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INJURY ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
POLYCYSTIC OVARIES ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RASH ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
AMBLYOPIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ANAL SPHINCTER ATONY ( 1 FDA reports)
ANISOMETROPIA ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BUNION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLOSTOMY ( 1 FDA reports)
COMA ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
DEAFNESS UNILATERAL ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DOUBLE STRANDED DNA ANTIBODY POSITIVE ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EUTHYROID SICK SYNDROME ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FALL ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INVESTIGATION ABNORMAL ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUPUS-LIKE SYNDROME ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS BACTERIAL ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
MONOCLONAL GAMMOPATHY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL OBSTRUCTION ( 1 FDA reports)
NEGLECT OF PERSONAL APPEARANCE ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR ERYTHEMA ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PENILE EXFOLIATION ( 1 FDA reports)
PERONEAL NERVE PALSY ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RECTAL FISSURE ( 1 FDA reports)
RECTAL PROLAPSE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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