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

PANCYTOPENIA ( 9 FDA reports)
ASTHENIA ( 5 FDA reports)
DYSPNOEA ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
INFECTION ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
RASH ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BLASTOMYCOSIS ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CUSHINGOID ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MAMMOGRAM ABNORMAL ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PH INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DOCUMENTED HYPERSENSITIVITY TO ADMINISTERED DRUG ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FALL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL CARCINOMA ( 1 FDA reports)
GASTROINTESTINAL NEOPLASM ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART SOUNDS ABNORMAL ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INJECTION SITE ABSCESS ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTATIC NEOPLASM ( 1 FDA reports)
METHAEMOGLOBINAEMIA ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA STAGE III ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANNICULITIS LOBULAR ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC NEOPLASM ( 1 FDA reports)
PERICARDIAL RUB ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POOR VENOUS ACCESS ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SALMONELLA SEPSIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TELANGIECTASIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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