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

ASPARTATE AMINOTRANSFERASE INCREASED ( 21 FDA reports)
LIVER DISORDER ( 17 FDA reports)
SEPSIS ( 17 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
PLATELET COUNT DECREASED ( 14 FDA reports)
RENAL FAILURE ACUTE ( 14 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 13 FDA reports)
MALAISE ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
STEVENS-JOHNSON SYNDROME ( 12 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 11 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 11 FDA reports)
BLOOD PRESSURE DECREASED ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
MULTI-ORGAN FAILURE ( 9 FDA reports)
PYREXIA ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
RASH ( 8 FDA reports)
ANOREXIA ( 7 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
NEUTROPENIA ( 7 FDA reports)
PAIN ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 7 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 6 FDA reports)
PROTHROMBIN TIME PROLONGED ( 6 FDA reports)
STAPHYLOCOCCAL INFECTION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
ASCITES ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DISEASE PROGRESSION ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HEPATITIS ACUTE ( 5 FDA reports)
HYPERCAPNIA ( 5 FDA reports)
INFECTION ( 5 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
SHOCK ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BODY TEMPERATURE INCREASED ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DRUG ERUPTION ( 4 FDA reports)
DYSPNOEA ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
MELAENA ( 4 FDA reports)
METASTASIS ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
PAINFUL RESPIRATION ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PROLONGED EXPIRATION ( 4 FDA reports)
SHOCK HYPOGLYCAEMIC ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EYE DISCHARGE ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HYPONATRAEMIA ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CHILLS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 2 FDA reports)
ERYTHEMA ANNULARE ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATITIS A POSITIVE ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OVARIAN CANCER ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCREATIC HAEMORRHAGE ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
ARM AMPUTATION ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COMA ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DIABETIC NEPHROPATHY ( 1 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELEVATED MOOD ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOD POISONING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATOBILIARY INFECTION ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INTERCOSTAL NEURALGIA ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LIP PAIN ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH SCALY ( 1 FDA reports)
RED BLOOD CELL ABNORMALITY ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC MYCOSIS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TRACHEAL DEVIATION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULAR STENOSIS ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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