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

BLOOD PRESSURE DECREASED ( 7 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
LIVER DISORDER ( 4 FDA reports)
MALAISE ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RESPIRATORY FAILURE ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
HAEMORRHAGIC DIATHESIS ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RASH ( 2 FDA reports)
SUFFOCATION FEELING ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
WATER INTOXICATION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL WALL ABSCESS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APATHY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BASOPHIL COUNT DECREASED ( 1 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORNEAL PERFORATION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CSF CELL COUNT INCREASED ( 1 FDA reports)
CSF PROTEIN ABNORMAL ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
KERATITIS FUNGAL ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP DISCOLOURATION ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYCOTIC CORNEAL ULCER ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEURILEMMOMA ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PITYRIASIS LICHENOIDES ET VARIOLIFORMIS ACUTA ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POST PROCEDURAL PAIN ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)

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