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

DERMAL CYST ( 8 FDA reports)
INFECTION ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
NEOPLASM MALIGNANT ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
DEATH ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
ENTEROCOLITIS ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 3 FDA reports)
PSEUDOMONAL SEPSIS ( 3 FDA reports)
SMALL INTESTINAL HAEMORRHAGE ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MALABSORPTION ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
ZINC DEFICIENCY ( 2 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
POSTICTAL STATE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
SHOCK ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
TINEA PEDIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)

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