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

PARKINSONISM ( 16 FDA reports)
DYSPNOEA ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
LIVER DISORDER ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 7 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
INTERSTITIAL LUNG DISEASE ( 6 FDA reports)
PLATELET COUNT DECREASED ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 6 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 6 FDA reports)
DEATH ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
INFECTION ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
BLOOD IRON DECREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BURSITIS ( 4 FDA reports)
CELLULITIS ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DEPRESSED MOOD ( 4 FDA reports)
DEPRESSION SUICIDAL ( 4 FDA reports)
GASTRIC ULCER ( 4 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
IRON DEFICIENCY ANAEMIA ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
RASH ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
SERUM FERRITIN DECREASED ( 4 FDA reports)
TONGUE ULCERATION ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
ALOPECIA ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
MALAISE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
VULVAL ULCERATION ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AORTIC VALVE STENOSIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
COLONIC POLYP ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DIVERTICULAR PERFORATION ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FEELING GUILTY ( 2 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPH NODE TUBERCULOSIS ( 2 FDA reports)
MELAS SYNDROME ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SKIN DISCOMFORT ( 2 FDA reports)
SNEEZING ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALCOHOLIC LIVER DISEASE ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAL PROLAPSE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BIRTH MARK ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BREAST OEDEMA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
COLITIS COLLAGENOUS ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIPLEGIA ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPIDERMAL GROWTH FACTOR RECEPTOR INCREASED ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
FACIAL SPASM ( 1 FDA reports)
FALL ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLAMMATORY CARCINOMA OF THE BREAST ( 1 FDA reports)
INJURY ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OESTROGEN RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PROGESTERONE RECEPTOR ASSAY POSITIVE ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSEUDOALDOSTERONISM ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETRACTED NIPPLE ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
ZYGOMYCOSIS ( 1 FDA reports)

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