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

NEUTROPENIA ( 28 FDA reports)
PYREXIA ( 25 FDA reports)
RESPIRATORY FAILURE ( 25 FDA reports)
SEPSIS ( 25 FDA reports)
RENAL FAILURE ACUTE ( 21 FDA reports)
RENAL IMPAIRMENT ( 19 FDA reports)
INSOMNIA ( 18 FDA reports)
NAUSEA ( 18 FDA reports)
FEBRILE NEUTROPENIA ( 17 FDA reports)
PANCYTOPENIA ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
RENAL FAILURE ( 17 FDA reports)
HYPOTENSION ( 16 FDA reports)
HEADACHE ( 15 FDA reports)
MULTI-ORGAN FAILURE ( 14 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 13 FDA reports)
ANAEMIA ( 13 FDA reports)
DISEASE PROGRESSION ( 13 FDA reports)
FATIGUE ( 13 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 12 FDA reports)
DIARRHOEA ( 12 FDA reports)
DIZZINESS ( 12 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 12 FDA reports)
NEUTROPHIL COUNT DECREASED ( 12 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
ABDOMINAL PAIN ( 11 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 11 FDA reports)
DRUG RESISTANCE ( 11 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
HYPONATRAEMIA ( 11 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 10 FDA reports)
DEATH ( 10 FDA reports)
DISTURBANCE IN ATTENTION ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
MALAISE ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
SEPTIC SHOCK ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
HEPATIC FAILURE ( 9 FDA reports)
HERPES ZOSTER ( 9 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
PLATELET COUNT DECREASED ( 9 FDA reports)
THROMBOCYTOPENIA ( 9 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
BACK INJURY ( 8 FDA reports)
CARDIAC FAILURE ( 8 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
COMMUNICATION DISORDER ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
DRUG INTERACTION ( 8 FDA reports)
FLUID RETENTION ( 8 FDA reports)
GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
HAEMOPTYSIS ( 8 FDA reports)
ILL-DEFINED DISORDER ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
JOINT INJURY ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PSEUDOMONAL SEPSIS ( 8 FDA reports)
SCIATIC NERVE INJURY ( 8 FDA reports)
THINKING ABNORMAL ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
FUNGAL INFECTION ( 7 FDA reports)
HALLUCINATION, AUDITORY ( 7 FDA reports)
HALLUCINATION, VISUAL ( 7 FDA reports)
NEUTROPENIC SEPSIS ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
ABDOMINAL DISTENSION ( 6 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CEREBRAL HAEMORRHAGE ( 6 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA TRANSFORMATION ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
CONSTIPATION ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DILATATION INTRAHEPATIC DUCT ACQUIRED ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
INFECTION ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
VOMITING ( 6 FDA reports)
ALOPECIA ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 5 FDA reports)
CYSTITIS HAEMORRHAGIC ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
FALL ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEPATOTOXICITY ( 5 FDA reports)
HERPES VIRUS INFECTION ( 5 FDA reports)
HYPOKALAEMIA ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
ORAL DISORDER ( 5 FDA reports)
PAIN ( 5 FDA reports)
RASH ( 5 FDA reports)
SYNCOPE ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 5 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLINDNESS ( 4 FDA reports)
BLOOD AMYLASE INCREASED ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CYSTITIS VIRAL ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
ENCEPHALITIS ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
MENINGITIS ASEPTIC ( 4 FDA reports)
OXYGEN SATURATION DECREASED ( 4 FDA reports)
PARAINFLUENZAE VIRUS INFECTION ( 4 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 4 FDA reports)
SOPOR ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
STREPTOCOCCAL INFECTION ( 4 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
ANTIPHOSPHOLIPID SYNDROME ( 3 FDA reports)
ANURIA ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHOROIDAL NEOVASCULARISATION ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
ECTOPIC PREGNANCY ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENGRAFT FAILURE ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEPATIC NECROSIS ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
INTERLEUKIN LEVEL INCREASED ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
MUCOSAL INFLAMMATION ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYOPATHY ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NEUROPSYCHIATRIC LUPUS ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 3 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 3 FDA reports)
PREGNANCY WITH IMPLANT CONTRACEPTIVE ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL FAILURE CHRONIC ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TREATMENT FAILURE ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASOCIAL BEHAVIOUR ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BONE ATROPHY ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
BRADYCARDIA ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CAECITIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL FUNGAL INFECTION ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CITROBACTER SEPSIS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 2 FDA reports)
COAGULATION TIME PROLONGED ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMA ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
COUGH ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOLLICULITIS ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INGUINAL HERNIA REPAIR ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIVER INJURY ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEUTROPHIL PELGER-HUET ANOMALY PRESENT ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PELVIC PAIN ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PITUITARY-DEPENDENT CUSHING'S SYNDROME ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 2 FDA reports)
PNEUMONITIS ( 2 FDA reports)
POST HERPETIC NEURALGIA ( 2 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA RECURRENT ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
ROTATOR CUFF SYNDROME ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SUICIDAL BEHAVIOUR ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TONGUE PARALYSIS ( 2 FDA reports)
TRANSPLANT FAILURE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS BACTERIAL ( 1 FDA reports)
ACANTHAMOEBA INFECTION ( 1 FDA reports)
ACARODERMATITIS ( 1 FDA reports)
ACTINIC KERATOSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ( 1 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMAUROSIS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOTENSIN CONVERTING ENZYME INCREASED ( 1 FDA reports)
ANORGASMIA ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APRAXIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLADDER OBSTRUCTION ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE ABSCESS ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPNEUMONIA ( 1 FDA reports)
C-REACTIVE PROTEIN ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC TAMPONADE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLECTOMY TOTAL ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONGENITAL HERPES SIMPLEX INFECTION ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORYNEBACTERIUM INFECTION ( 1 FDA reports)
CREATININE RENAL CLEARANCE ABNORMAL ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS ENTERITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA INFECTIOUS ( 1 FDA reports)
DIASTOLIC DYSFUNCTION ( 1 FDA reports)
DIASTOLIC HYPOTENSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DETOXIFICATION ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EJECTION FRACTION ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOCCAL SEPSIS ( 1 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 1 FDA reports)
EOSINOPHIL COUNT DECREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXPOSURE DURING BREAST FEEDING ( 1 FDA reports)
EXTRANODAL MARGINAL ZONE B-CELL LYMPHOMA (MALT TYPE) ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FRACTURED ISCHIUM ( 1 FDA reports)
GALLBLADDER POLYP ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROENTERITIS NOROVIRUS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL ULCERATION ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRANULOMA SKIN ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATOSPLENOMEGALY ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HYPERAMMONAEMIA ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOTHERMIA NEONATAL ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE INFECTION ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INJECTION SITE EXFOLIATION ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE SCAB ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKAEMIC INFILTRATION BRAIN ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIVEDO RETICULARIS ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MACROPHAGE ACTIVATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MANTLE CELL LYMPHOMA ( 1 FDA reports)
MATERNAL EXPOSURE TIMING UNSPECIFIED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROBLASTOMA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA ( 1 FDA reports)
NEUROPATHIC ULCER ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PETIT MAL EPILEPSY ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
POLYOMAVIRUS-ASSOCIATED NEPHROPATHY ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
POROCARCINOMA ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY MICROEMBOLI ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PURPURA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
REPERFUSION ARRHYTHMIA ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SIGHT DISABILITY ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STENOTROPHOMONAS SEPSIS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THALAMIC INFARCTION ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSFUSION-RELATED ACUTE LUNG INJURY ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRIGEMINAL PALSY ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
TUMOUR LYSIS SYNDROME ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UVEITIS ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
WARM TYPE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use