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

PYREXIA ( 322 FDA reports)
SEPSIS ( 220 FDA reports)
RESPIRATORY FAILURE ( 196 FDA reports)
DRUG INEFFECTIVE ( 192 FDA reports)
MULTI-ORGAN FAILURE ( 184 FDA reports)
PNEUMONIA ( 176 FDA reports)
FEBRILE NEUTROPENIA ( 168 FDA reports)
RENAL FAILURE ACUTE ( 151 FDA reports)
DIARRHOEA ( 144 FDA reports)
RENAL FAILURE ( 141 FDA reports)
BLOOD CREATININE INCREASED ( 132 FDA reports)
THROMBOCYTOPENIA ( 132 FDA reports)
ASPERGILLOSIS ( 127 FDA reports)
ANAEMIA ( 123 FDA reports)
HYPOTENSION ( 122 FDA reports)
NEUTROPENIA ( 122 FDA reports)
DYSPNOEA ( 120 FDA reports)
DRUG INTERACTION ( 119 FDA reports)
HYPOKALAEMIA ( 115 FDA reports)
NAUSEA ( 113 FDA reports)
PANCYTOPENIA ( 107 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 104 FDA reports)
RENAL IMPAIRMENT ( 104 FDA reports)
VOMITING ( 104 FDA reports)
DEATH ( 100 FDA reports)
SEPTIC SHOCK ( 96 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 91 FDA reports)
CONDITION AGGRAVATED ( 87 FDA reports)
LEUKOPENIA ( 85 FDA reports)
PLATELET COUNT DECREASED ( 85 FDA reports)
PLEURAL EFFUSION ( 85 FDA reports)
TACHYCARDIA ( 83 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 82 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 82 FDA reports)
INFECTION ( 81 FDA reports)
CARDIAC ARREST ( 80 FDA reports)
JAUNDICE ( 80 FDA reports)
FUNGAL INFECTION ( 79 FDA reports)
GRAFT VERSUS HOST DISEASE ( 76 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 75 FDA reports)
HEPATIC ENZYME INCREASED ( 74 FDA reports)
BLOOD BILIRUBIN INCREASED ( 72 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 70 FDA reports)
LIVER DISORDER ( 70 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 67 FDA reports)
AGRANULOCYTOSIS ( 62 FDA reports)
HYPERTENSION ( 62 FDA reports)
ABDOMINAL PAIN ( 61 FDA reports)
CARDIAC FAILURE ( 61 FDA reports)
DEHYDRATION ( 61 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 61 FDA reports)
HEADACHE ( 61 FDA reports)
HAEMOGLOBIN DECREASED ( 59 FDA reports)
PULMONARY HAEMORRHAGE ( 59 FDA reports)
LUNG INFECTION ( 58 FDA reports)
CANDIDIASIS ( 57 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 57 FDA reports)
DISEASE PROGRESSION ( 50 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 50 FDA reports)
CHILLS ( 49 FDA reports)
CHOLESTASIS ( 49 FDA reports)
RASH ( 49 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 48 FDA reports)
DIZZINESS ( 48 FDA reports)
NEPHROPATHY TOXIC ( 48 FDA reports)
STAPHYLOCOCCAL INFECTION ( 48 FDA reports)
WEIGHT DECREASED ( 48 FDA reports)
CONFUSIONAL STATE ( 47 FDA reports)
DRUG RESISTANCE ( 47 FDA reports)
STOMATITIS ( 47 FDA reports)
BONE MARROW FAILURE ( 46 FDA reports)
COUGH ( 46 FDA reports)
METABOLIC ACIDOSIS ( 45 FDA reports)
PAIN ( 45 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 44 FDA reports)
CONVULSION ( 44 FDA reports)
HAEMORRHAGE ( 43 FDA reports)
MUCOSAL INFLAMMATION ( 43 FDA reports)
SHOCK ( 43 FDA reports)
ENCEPHALOPATHY ( 41 FDA reports)
HEPATOTOXICITY ( 41 FDA reports)
RESPIRATORY DISTRESS ( 41 FDA reports)
ACUTE MONOCYTIC LEUKAEMIA ( 40 FDA reports)
DRUG TOXICITY ( 40 FDA reports)
OEDEMA PERIPHERAL ( 40 FDA reports)
CARDIO-RESPIRATORY ARREST ( 39 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 38 FDA reports)
ARRHYTHMIA ( 38 FDA reports)
HYPOXIA ( 37 FDA reports)
ZYGOMYCOSIS ( 37 FDA reports)
BLOOD UREA INCREASED ( 36 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 36 FDA reports)
DIALYSIS ( 36 FDA reports)
DRUG LEVEL INCREASED ( 36 FDA reports)
MYOCARDIAL INFARCTION ( 36 FDA reports)
URINARY TRACT INFECTION ( 36 FDA reports)
ATRIAL FIBRILLATION ( 35 FDA reports)
CEREBRAL HAEMORRHAGE ( 35 FDA reports)
ENTEROCOCCAL INFECTION ( 35 FDA reports)
FATIGUE ( 35 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 35 FDA reports)
MENINGITIS CRYPTOCOCCAL ( 35 FDA reports)
PNEUMONITIS ( 35 FDA reports)
PULMONARY OEDEMA ( 35 FDA reports)
BLOOD PRESSURE DECREASED ( 34 FDA reports)
HYPERKALAEMIA ( 34 FDA reports)
CRYPTOCOCCOSIS ( 33 FDA reports)
FUNGUS CULTURE POSITIVE ( 33 FDA reports)
HEPATIC FAILURE ( 33 FDA reports)
OEDEMA ( 33 FDA reports)
TRANSPLANT REJECTION ( 33 FDA reports)
DISEASE RECURRENCE ( 32 FDA reports)
HYPONATRAEMIA ( 31 FDA reports)
INTERSTITIAL LUNG DISEASE ( 31 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 31 FDA reports)
SOMNOLENCE ( 31 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 30 FDA reports)
COMA ( 30 FDA reports)
LUNG INFILTRATION ( 30 FDA reports)
LYMPHADENOPATHY ( 30 FDA reports)
AGITATION ( 29 FDA reports)
BACTERIAL INFECTION ( 29 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 29 FDA reports)
HYPERBILIRUBINAEMIA ( 29 FDA reports)
HYPERSENSITIVITY ( 29 FDA reports)
PERICARDIAL EFFUSION ( 29 FDA reports)
PRURITUS ( 29 FDA reports)
PNEUMONIA FUNGAL ( 28 FDA reports)
WEIGHT INCREASED ( 28 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 27 FDA reports)
CIRCULATORY COLLAPSE ( 27 FDA reports)
GRAND MAL CONVULSION ( 27 FDA reports)
HAEMOPTYSIS ( 27 FDA reports)
HYPOALBUMINAEMIA ( 27 FDA reports)
MEDICATION ERROR ( 27 FDA reports)
ORAL CANDIDIASIS ( 27 FDA reports)
PNEUMOTHORAX ( 27 FDA reports)
STEVENS-JOHNSON SYNDROME ( 27 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 27 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 26 FDA reports)
HAEMATOCHEZIA ( 26 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 26 FDA reports)
LYMPHOCELE ( 26 FDA reports)
OXYGEN SATURATION DECREASED ( 26 FDA reports)
PANCREATITIS ( 26 FDA reports)
CHEST PAIN ( 25 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 25 FDA reports)
ERYTHEMA ( 25 FDA reports)
NECROSIS ( 25 FDA reports)
PSEUDOMONAS INFECTION ( 25 FDA reports)
THERAPY NON-RESPONDER ( 25 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 24 FDA reports)
BRAIN OEDEMA ( 24 FDA reports)
BRONCHITIS ( 24 FDA reports)
FLUID OVERLOAD ( 24 FDA reports)
HAEMODIALYSIS ( 24 FDA reports)
HERPES ZOSTER ( 24 FDA reports)
ILL-DEFINED DISORDER ( 24 FDA reports)
LUNG DISORDER ( 24 FDA reports)
SPLENOMEGALY ( 24 FDA reports)
BLOOD CULTURE POSITIVE ( 23 FDA reports)
BLOOD SODIUM DECREASED ( 23 FDA reports)
BRADYCARDIA ( 23 FDA reports)
HEPATOMEGALY ( 23 FDA reports)
INFUSION RELATED REACTION ( 23 FDA reports)
LEUKAEMIA ( 23 FDA reports)
LOSS OF CONSCIOUSNESS ( 23 FDA reports)
NO THERAPEUTIC RESPONSE ( 23 FDA reports)
OLIGURIA ( 23 FDA reports)
PULMONARY EMBOLISM ( 23 FDA reports)
RHABDOMYOLYSIS ( 23 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 23 FDA reports)
ASCITES ( 22 FDA reports)
ASTHENIA ( 22 FDA reports)
HISTOPLASMOSIS ( 22 FDA reports)
LEUKOCYTOSIS ( 22 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 22 FDA reports)
PANCREATITIS ACUTE ( 22 FDA reports)
SINUSITIS ( 22 FDA reports)
BLOOD ALBUMIN DECREASED ( 21 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 21 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 21 FDA reports)
CELLULITIS ( 21 FDA reports)
CHOLELITHIASIS ( 21 FDA reports)
COAGULOPATHY ( 21 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 21 FDA reports)
FUSARIUM INFECTION ( 21 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 21 FDA reports)
MALAISE ( 21 FDA reports)
PATHOGEN RESISTANCE ( 21 FDA reports)
VENOOCCLUSIVE DISEASE ( 21 FDA reports)
DERMAL CYST ( 20 FDA reports)
DEVICE RELATED INFECTION ( 20 FDA reports)
ENDOCARDITIS ( 20 FDA reports)
EPILEPSY ( 20 FDA reports)
GASTROENTERITIS ( 20 FDA reports)
NEUTROPHIL COUNT DECREASED ( 20 FDA reports)
OVERDOSE ( 20 FDA reports)
PAIN IN EXTREMITY ( 20 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 20 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 20 FDA reports)
RESPIRATORY DISORDER ( 20 FDA reports)
BLISTER ( 19 FDA reports)
BODY TEMPERATURE INCREASED ( 19 FDA reports)
BONE PAIN ( 19 FDA reports)
DEPRESSION ( 19 FDA reports)
DIABETES MELLITUS ( 19 FDA reports)
HAEMATOCRIT DECREASED ( 19 FDA reports)
HYPERHIDROSIS ( 19 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 19 FDA reports)
SEPTIC EMBOLUS ( 19 FDA reports)
SUBDURAL HAEMATOMA ( 19 FDA reports)
SYSTEMIC CANDIDA ( 19 FDA reports)
TACHYPNOEA ( 19 FDA reports)
TRANSAMINASES INCREASED ( 19 FDA reports)
ACUTE RESPIRATORY FAILURE ( 18 FDA reports)
ANXIETY ( 18 FDA reports)
BACK PAIN ( 18 FDA reports)
BRAIN ABSCESS ( 18 FDA reports)
CYSTITIS HAEMORRHAGIC ( 18 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 18 FDA reports)
GASTRITIS ( 18 FDA reports)
HAEMATURIA ( 18 FDA reports)
HYPOMAGNESAEMIA ( 18 FDA reports)
MENTAL STATUS CHANGES ( 18 FDA reports)
VASCULITIS ( 18 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 18 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 17 FDA reports)
BACTERAEMIA ( 17 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 17 FDA reports)
CYTOLYTIC HEPATITIS ( 17 FDA reports)
DECREASED APPETITE ( 17 FDA reports)
ELECTROLYTE IMBALANCE ( 17 FDA reports)
FALL ( 17 FDA reports)
GASTROINTESTINAL DISORDER ( 17 FDA reports)
HEPATITIS CHOLESTATIC ( 17 FDA reports)
NERVOUS SYSTEM DISORDER ( 17 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 17 FDA reports)
PARAESTHESIA ( 17 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 17 FDA reports)
SKIN EXFOLIATION ( 17 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 17 FDA reports)
TORSADE DE POINTES ( 17 FDA reports)
TREMOR ( 17 FDA reports)
ABDOMINAL PAIN UPPER ( 16 FDA reports)
ANOREXIA ( 16 FDA reports)
BACTERIAL SEPSIS ( 16 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 16 FDA reports)
BLOOD PRESSURE INCREASED ( 16 FDA reports)
DRUG HYPERSENSITIVITY ( 16 FDA reports)
DYSPHAGIA ( 16 FDA reports)
EPISTAXIS ( 16 FDA reports)
FUNGAL SEPSIS ( 16 FDA reports)
GASTROINTESTINAL TOXICITY ( 16 FDA reports)
HEPATIC NECROSIS ( 16 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 16 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 16 FDA reports)
KLEBSIELLA INFECTION ( 16 FDA reports)
LEUKAEMIA RECURRENT ( 16 FDA reports)
MITRAL VALVE INCOMPETENCE ( 16 FDA reports)
MUSCULAR WEAKNESS ( 16 FDA reports)
RENAL DISORDER ( 16 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 16 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 16 FDA reports)
URINARY RETENTION ( 16 FDA reports)
URTICARIA ( 16 FDA reports)
BLINDNESS ( 15 FDA reports)
DEAFNESS ( 15 FDA reports)
ENCEPHALITIS ( 15 FDA reports)
ESCHERICHIA INFECTION ( 15 FDA reports)
FEELING ABNORMAL ( 15 FDA reports)
HAEMATEMESIS ( 15 FDA reports)
HAEMOLYTIC ANAEMIA ( 15 FDA reports)
HEPATIC STEATOSIS ( 15 FDA reports)
HYPOPHAGIA ( 15 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 15 FDA reports)
MYOCARDIAL ISCHAEMIA ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
SKIN LESION ( 15 FDA reports)
VENTRICULAR FIBRILLATION ( 15 FDA reports)
VENTRICULAR TACHYCARDIA ( 15 FDA reports)
ABSCESS ( 14 FDA reports)
ANGIOEDEMA ( 14 FDA reports)
ARTHRALGIA ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 14 FDA reports)
CANDIDA SEPSIS ( 14 FDA reports)
CARDIOGENIC SHOCK ( 14 FDA reports)
CARDIOMEGALY ( 14 FDA reports)
CEREBRAL ISCHAEMIA ( 14 FDA reports)
DRUG INTOLERANCE ( 14 FDA reports)
EYE PAIN ( 14 FDA reports)
FUNGAL ENDOCARDITIS ( 14 FDA reports)
GENERALISED OEDEMA ( 14 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 14 FDA reports)
HEMIPLEGIA ( 14 FDA reports)
HEPATITIS ( 14 FDA reports)
HYPERGLYCAEMIA ( 14 FDA reports)
HYPERNATRAEMIA ( 14 FDA reports)
LEUKOENCEPHALOPATHY ( 14 FDA reports)
LIP EROSION ( 14 FDA reports)
MENINGITIS ( 14 FDA reports)
MUCORMYCOSIS ( 14 FDA reports)
NEUROPATHY PERIPHERAL ( 14 FDA reports)
NEUTROPENIC SEPSIS ( 14 FDA reports)
POST PROCEDURAL BILE LEAK ( 14 FDA reports)
SEBORRHOEIC DERMATITIS ( 14 FDA reports)
VISUAL ACUITY REDUCED ( 14 FDA reports)
CHOLECYSTITIS ( 13 FDA reports)
COLITIS ( 13 FDA reports)
CONSTIPATION ( 13 FDA reports)
DELIRIUM ( 13 FDA reports)
DISORIENTATION ( 13 FDA reports)
ENTEROCOCCAL SEPSIS ( 13 FDA reports)
EOSINOPHILIA ( 13 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
HALLUCINATION ( 13 FDA reports)
HEPATITIS B ( 13 FDA reports)
HYPERAMMONAEMIA ( 13 FDA reports)
LACTIC ACIDOSIS ( 13 FDA reports)
PALLOR ( 13 FDA reports)
POST PROCEDURAL URINE LEAK ( 13 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 13 FDA reports)
PULMONARY HYPERTENSION ( 13 FDA reports)
RASH MACULO-PAPULAR ( 13 FDA reports)
RENAL TUBULAR DISORDER ( 13 FDA reports)
SPUTUM CULTURE POSITIVE ( 13 FDA reports)
SYSTEMIC MYCOSIS ( 13 FDA reports)
TRANSPLANT FAILURE ( 13 FDA reports)
VISCERAL LEISHMANIASIS ( 13 FDA reports)
ABDOMINAL DISTENSION ( 12 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 12 FDA reports)
ANURIA ( 12 FDA reports)
BLOOD POTASSIUM DECREASED ( 12 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
CONJUNCTIVITIS ( 12 FDA reports)
DRUG EFFECT DECREASED ( 12 FDA reports)
ENGRAFTMENT SYNDROME ( 12 FDA reports)
EYE INFECTION FUNGAL ( 12 FDA reports)
HICCUPS ( 12 FDA reports)
HYPERPYREXIA ( 12 FDA reports)
INTESTINAL INFARCTION ( 12 FDA reports)
LIVER INJURY ( 12 FDA reports)
LOBAR PNEUMONIA ( 12 FDA reports)
OCULAR HYPERAEMIA ( 12 FDA reports)
PAPILLOEDEMA ( 12 FDA reports)
PERITONITIS ( 12 FDA reports)
POST PROCEDURAL COMPLICATION ( 12 FDA reports)
PURULENT DISCHARGE ( 12 FDA reports)
URINE OUTPUT DECREASED ( 12 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 12 FDA reports)
ACCIDENTAL OVERDOSE ( 11 FDA reports)
ADENOVIRUS INFECTION ( 11 FDA reports)
CAECITIS ( 11 FDA reports)
CLOSTRIDIAL INFECTION ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
DYSARTHRIA ( 11 FDA reports)
ENTEROCOLITIS ( 11 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 11 FDA reports)
FUNGAEMIA ( 11 FDA reports)
FUNGAL SKIN INFECTION ( 11 FDA reports)
HALLUCINATION, VISUAL ( 11 FDA reports)
HYPERLIPIDAEMIA ( 11 FDA reports)
HYPERURICAEMIA ( 11 FDA reports)
ILEUS ( 11 FDA reports)
ILEUS PARALYTIC ( 11 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 11 FDA reports)
PLEURISY ( 11 FDA reports)
PSEUDOMONAL SEPSIS ( 11 FDA reports)
PULMONARY CONGESTION ( 11 FDA reports)
RECTAL ULCER ( 11 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 11 FDA reports)
RENAL TUBULAR NECROSIS ( 11 FDA reports)
RESTLESSNESS ( 11 FDA reports)
STEM CELL TRANSPLANT ( 11 FDA reports)
STENOTROPHOMONAS INFECTION ( 11 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 11 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 11 FDA reports)
VISUAL IMPAIRMENT ( 11 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 10 FDA reports)
ANGINA PECTORIS ( 10 FDA reports)
APLASTIC ANAEMIA ( 10 FDA reports)
BONE MARROW TOXICITY ( 10 FDA reports)
CARDIAC MURMUR ( 10 FDA reports)
CARDIAC VALVE VEGETATION ( 10 FDA reports)
CATHETER RELATED INFECTION ( 10 FDA reports)
DRUG LEVEL DECREASED ( 10 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 10 FDA reports)
FEBRILE BONE MARROW APLASIA ( 10 FDA reports)
HAEMODYNAMIC INSTABILITY ( 10 FDA reports)
HAEMOLYSIS ( 10 FDA reports)
HAEMORRHAGIC DIATHESIS ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
HEPATIC CIRRHOSIS ( 10 FDA reports)
HEPATIC LESION ( 10 FDA reports)
HIV INFECTION ( 10 FDA reports)
HYPERTHERMIA ( 10 FDA reports)
IMPAIRED HEALING ( 10 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 10 FDA reports)
INFLUENZA ( 10 FDA reports)
ISCHAEMIC STROKE ( 10 FDA reports)
KAPOSI'S SARCOMA ( 10 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 10 FDA reports)
LIVER TRANSPLANT ( 10 FDA reports)
NEUROTOXICITY ( 10 FDA reports)
ORAL HERPES ( 10 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 10 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 10 FDA reports)
RASH ERYTHEMATOUS ( 10 FDA reports)
RASH MACULAR ( 10 FDA reports)
TUMOUR LYSIS SYNDROME ( 10 FDA reports)
UROSEPSIS ( 10 FDA reports)
VIRAL INFECTION ( 10 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 9 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 9 FDA reports)
BRONCHOPNEUMONIA ( 9 FDA reports)
CAPILLARY LEAK SYNDROME ( 9 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 9 FDA reports)
COLD SWEAT ( 9 FDA reports)
CORONARY ARTERY ANEURYSM ( 9 FDA reports)
CYSTITIS ( 9 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 9 FDA reports)
FLUSHING ( 9 FDA reports)
GASTRIC ULCER ( 9 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 9 FDA reports)
HEMIPARESIS ( 9 FDA reports)
HYDROCEPHALUS ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
IDIOPATHIC PNEUMONIA SYNDROME ( 9 FDA reports)
JOINT SWELLING ( 9 FDA reports)
MECHANICAL VENTILATION ( 9 FDA reports)
MUCOUS MEMBRANE DISORDER ( 9 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 9 FDA reports)
MYELODYSPLASTIC SYNDROME ( 9 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 9 FDA reports)
OFF LABEL USE ( 9 FDA reports)
PARADOXICAL DRUG REACTION ( 9 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 9 FDA reports)
PNEUMONIA ASPIRATION ( 9 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 9 FDA reports)
PORTAL HYPERTENSION ( 9 FDA reports)
PURPURA ( 9 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 9 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 9 FDA reports)
SERUM FERRITIN INCREASED ( 9 FDA reports)
SHOCK HAEMORRHAGIC ( 9 FDA reports)
STATUS EPILEPTICUS ( 9 FDA reports)
SUBCUTANEOUS NODULE ( 9 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 9 FDA reports)
TREATMENT NONCOMPLIANCE ( 9 FDA reports)
UNEVALUABLE EVENT ( 9 FDA reports)
VARICES OESOPHAGEAL ( 9 FDA reports)
VENTRICULAR HYPERTROPHY ( 9 FDA reports)
WHEEZING ( 9 FDA reports)
ACIDOSIS ( 8 FDA reports)
ACINETOBACTER INFECTION ( 8 FDA reports)
ACUTE ABDOMEN ( 8 FDA reports)
ACUTE HEPATIC FAILURE ( 8 FDA reports)
ACUTE PULMONARY OEDEMA ( 8 FDA reports)
AGGRESSION ( 8 FDA reports)
ANAPHYLACTIC SHOCK ( 8 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
BONE MARROW TRANSPLANT ( 8 FDA reports)
CARDIOMYOPATHY ( 8 FDA reports)
CARDIOPULMONARY FAILURE ( 8 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
CHEST DISCOMFORT ( 8 FDA reports)
DIVERTICULITIS ( 8 FDA reports)
DIZZINESS POSTURAL ( 8 FDA reports)
FACE OEDEMA ( 8 FDA reports)
GAZE PALSY ( 8 FDA reports)
HYPERCALCAEMIA ( 8 FDA reports)
HYPOCALCAEMIA ( 8 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 8 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 8 FDA reports)
INFLAMMATION ( 8 FDA reports)
INJURY ( 8 FDA reports)
INSOMNIA ( 8 FDA reports)
KERATITIS FUNGAL ( 8 FDA reports)
LABORATORY TEST ABNORMAL ( 8 FDA reports)
MALNUTRITION ( 8 FDA reports)
NEURALGIA ( 8 FDA reports)
PANCREATIC DISORDER ( 8 FDA reports)
PARONYCHIA ( 8 FDA reports)
PROTHROMBIN TIME PROLONGED ( 8 FDA reports)
PSYCHOTIC DISORDER ( 8 FDA reports)
PULMONARY FIBROSIS ( 8 FDA reports)
RASH PAPULAR ( 8 FDA reports)
RENAL INJURY ( 8 FDA reports)
SKIN ULCER ( 8 FDA reports)
SUDDEN DEATH ( 8 FDA reports)
TREATMENT FAILURE ( 8 FDA reports)
URINARY INCONTINENCE ( 8 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 8 FDA reports)
VIRAL HAEMORRHAGIC CYSTITIS ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
WOUND INFECTION ( 8 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
APLASIA ( 7 FDA reports)
ARTERIAL HAEMORRHAGE ( 7 FDA reports)
ARTHRITIS ( 7 FDA reports)
ARTHRITIS BACTERIAL ( 7 FDA reports)
ARTHROPATHY ( 7 FDA reports)
ASPERGILLOMA ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 7 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 7 FDA reports)
BONE MARROW DISORDER ( 7 FDA reports)
CARDIOTOXICITY ( 7 FDA reports)
CHRONIC ALLOGRAFT NEPHROPATHY ( 7 FDA reports)
COLLAPSE OF LUNG ( 7 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 7 FDA reports)
CULTURE URINE POSITIVE ( 7 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 7 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 7 FDA reports)
DRY SKIN ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
EMBOLISM ( 7 FDA reports)
ENCEPHALITIS VIRAL ( 7 FDA reports)
ENDOPHTHALMITIS ( 7 FDA reports)
ENTEROBACTER INFECTION ( 7 FDA reports)
FAECAL INCONTINENCE ( 7 FDA reports)
GRANULOMA ( 7 FDA reports)
HAEMATOTOXICITY ( 7 FDA reports)
HEART RATE DECREASED ( 7 FDA reports)
HEPATITIS C ( 7 FDA reports)
HEPATITIS TOXIC ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HEPATOSPLENOMEGALY ( 7 FDA reports)
HERPES SIMPLEX ( 7 FDA reports)
INTRACRANIAL HAEMATOMA ( 7 FDA reports)
JAUNDICE CHOLESTATIC ( 7 FDA reports)
LIVER ABSCESS ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
LYMPHADENITIS ( 7 FDA reports)
LYMPHOPENIA ( 7 FDA reports)
LYMPHOPROLIFERATIVE DISORDER ( 7 FDA reports)
METABOLIC ENCEPHALOPATHY ( 7 FDA reports)
NIKOLSKY'S SIGN ( 7 FDA reports)
OESOPHAGITIS ( 7 FDA reports)
ORAL INTAKE REDUCED ( 7 FDA reports)
ORAL MUCOSA EROSION ( 7 FDA reports)
OSTEOMYELITIS ( 7 FDA reports)
PHOTOPHOBIA ( 7 FDA reports)
PLEURAL ADHESION ( 7 FDA reports)
PRODUCTIVE COUGH ( 7 FDA reports)
PROTEIN TOTAL DECREASED ( 7 FDA reports)
PULMONARY MYCOSIS ( 7 FDA reports)
PYELONEPHRITIS ( 7 FDA reports)
RENAL TRANSPLANT ( 7 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 7 FDA reports)
SPUTUM INCREASED ( 7 FDA reports)
STREPTOCOCCAL INFECTION ( 7 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 7 FDA reports)
SURGERY ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
THERMAL BURN ( 7 FDA reports)
TUBERCULOSIS ( 7 FDA reports)
TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
VISUAL FIELD DEFECT ( 7 FDA reports)
ACNE ( 6 FDA reports)
ANAL EROSION ( 6 FDA reports)
BK VIRUS INFECTION ( 6 FDA reports)
BONE MARROW DEPRESSION ( 6 FDA reports)
BRAIN INJURY ( 6 FDA reports)
CACHEXIA ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CARDIAC TAMPONADE ( 6 FDA reports)
CARDIOVASCULAR DISORDER ( 6 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 6 FDA reports)
CHEILITIS ( 6 FDA reports)
CLONUS ( 6 FDA reports)
COMA HEPATIC ( 6 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 6 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 6 FDA reports)
CSF PROTEIN INCREASED ( 6 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 6 FDA reports)
DIABETES INSIPIDUS ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
EATING DISORDER ( 6 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 6 FDA reports)
EMOTIONAL DISTRESS ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 6 FDA reports)
ENGRAFT FAILURE ( 6 FDA reports)
EYE ROLLING ( 6 FDA reports)
EYELID OEDEMA ( 6 FDA reports)
FEAR ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 6 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 6 FDA reports)
GENITAL EROSION ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HAEMATOMA INFECTION ( 6 FDA reports)
HEMIANOPIA ( 6 FDA reports)
HEPATITIS ACUTE ( 6 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 6 FDA reports)
IMMUNOSUPPRESSION ( 6 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 6 FDA reports)
JC VIRUS INFECTION ( 6 FDA reports)
LIVER TRANSPLANT REJECTION ( 6 FDA reports)
MENINGISM ( 6 FDA reports)
MOUTH HAEMORRHAGE ( 6 FDA reports)
MOUTH ULCERATION ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
MYOCARDITIS ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
NEONATAL DISORDER ( 6 FDA reports)
NEUROLOGICAL SYMPTOM ( 6 FDA reports)
NONSPECIFIC REACTION ( 6 FDA reports)
ORGANISING PNEUMONIA ( 6 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 6 FDA reports)
PERSECUTORY DELUSION ( 6 FDA reports)
PHARYNGITIS ( 6 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
RALES ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RECTAL HAEMORRHAGE ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
SPLENIC INFARCTION ( 6 FDA reports)
STRESS ( 6 FDA reports)
STUPOR ( 6 FDA reports)
SYNCOPE ( 6 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 6 FDA reports)
URETERIC STENOSIS ( 6 FDA reports)
VENOUS THROMBOSIS ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 5 FDA reports)
ALVEOLITIS ALLERGIC ( 5 FDA reports)
ANAPHYLACTIC REACTION ( 5 FDA reports)
ANGIOPATHY ( 5 FDA reports)
APHASIA ( 5 FDA reports)
APLASIA PURE RED CELL ( 5 FDA reports)
APPENDICITIS ( 5 FDA reports)
AUTOIMMUNE DISORDER ( 5 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 5 FDA reports)
BLOOD AMYLASE INCREASED ( 5 FDA reports)
BLOOD BICARBONATE DECREASED ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD CREATINE INCREASED ( 5 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 5 FDA reports)
BRAIN DAMAGE ( 5 FDA reports)
CANDIDA PNEUMONIA ( 5 FDA reports)
CAROTID ARTERY THROMBOSIS ( 5 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 5 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 5 FDA reports)
CEREBELLAR SYNDROME ( 5 FDA reports)
CEREBRAL DISORDER ( 5 FDA reports)
CHEST X-RAY ABNORMAL ( 5 FDA reports)
CHOLANGITIS ( 5 FDA reports)
CHOLECYSTITIS ACUTE ( 5 FDA reports)
CITROBACTER INFECTION ( 5 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 5 FDA reports)
COCCIDIOIDOMYCOSIS ( 5 FDA reports)
COMPLICATIONS OF TRANSPLANT SURGERY ( 5 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 5 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
CYANOSIS ( 5 FDA reports)
DEEP VEIN THROMBOSIS ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG DISPENSING ERROR ( 5 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 5 FDA reports)
ECTHYMA ( 5 FDA reports)
EFFUSION ( 5 FDA reports)
ENTERITIS ( 5 FDA reports)
EPSTEIN-BARR VIRUS TEST POSITIVE ( 5 FDA reports)
EROSIVE OESOPHAGITIS ( 5 FDA reports)
FACIAL PALSY ( 5 FDA reports)
FLUID RETENTION ( 5 FDA reports)
FOLLICULITIS ( 5 FDA reports)
FOOT FRACTURE ( 5 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 5 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 5 FDA reports)
GRAFT DYSFUNCTION ( 5 FDA reports)
HALLUCINATIONS, MIXED ( 5 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 5 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
HYPOPYON ( 5 FDA reports)
INCORRECT DOSE ADMINISTERED ( 5 FDA reports)
INTERVERTEBRAL DISCITIS ( 5 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 5 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 5 FDA reports)
IRRITABILITY ( 5 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 5 FDA reports)
LIFE SUPPORT ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
MENTAL DISORDER ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
MUCOSAL EROSION ( 5 FDA reports)
MUCOSAL HAEMORRHAGE ( 5 FDA reports)
MULTIPLE MYELOMA ( 5 FDA reports)
MUSCLE ATROPHY ( 5 FDA reports)
MYCOBACTERIAL INFECTION ( 5 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 5 FDA reports)
NEOPLASM MALIGNANT ( 5 FDA reports)
NEPHROLITHIASIS ( 5 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
OPTIC ATROPHY ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
OSTEOPENIA ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PERIORBITAL OEDEMA ( 5 FDA reports)
PERIVASCULAR DERMATITIS ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
POLYNEUROPATHY ( 5 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
RESPIRATORY DEPRESSION ( 5 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY TRACT INFECTION ( 5 FDA reports)
RETINAL DETACHMENT ( 5 FDA reports)
RETINITIS ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
ROSACEA ( 5 FDA reports)
SEROTONIN SYNDROME ( 5 FDA reports)
SINUS TACHYCARDIA ( 5 FDA reports)
SINUSITIS ASPERGILLUS ( 5 FDA reports)
SINUSITIS FUNGAL ( 5 FDA reports)
SKIN DISORDER ( 5 FDA reports)
SKIN NODULE ( 5 FDA reports)
SPLENIC ABSCESS ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 5 FDA reports)
THALASSAEMIA ALPHA ( 5 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
TOXOPLASMOSIS ( 5 FDA reports)
TRICHOSPORON INFECTION ( 5 FDA reports)
ACANTHAMOEBA INFECTION ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
ADVERSE DRUG REACTION ( 4 FDA reports)
AKINESIA ( 4 FDA reports)
ALKALOSIS ( 4 FDA reports)
ANHEDONIA ( 4 FDA reports)
APATHY ( 4 FDA reports)
APPLICATION SITE REACTION ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
ATYPICAL MYCOBACTERIAL LYMPHADENITIS ( 4 FDA reports)
BACILLUS INFECTION ( 4 FDA reports)
BACTERIA STOOL IDENTIFIED ( 4 FDA reports)
BACTERIAL TOXAEMIA ( 4 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 4 FDA reports)
BILE DUCT OBSTRUCTION ( 4 FDA reports)
BLOOD BETA-D-GLUCAN ABNORMAL ( 4 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 4 FDA reports)
BLOOD URIC ACID INCREASED ( 4 FDA reports)
BONE MARROW TRANSPLANT REJECTION ( 4 FDA reports)
BRONCHIAL OBSTRUCTION ( 4 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 4 FDA reports)
CEREBRAL ASPERGILLOSIS ( 4 FDA reports)
CEREBRAL FUNGAL INFECTION ( 4 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 4 FDA reports)
CHOKING ( 4 FDA reports)
COLITIS ULCERATIVE ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONGENITAL ANAEMIA ( 4 FDA reports)
CONGENITAL CORONARY ARTERY MALFORMATION ( 4 FDA reports)
CONGENITAL PULMONARY HYPERTENSION ( 4 FDA reports)
CORNEAL OEDEMA ( 4 FDA reports)
CORNEAL OPACITY ( 4 FDA reports)
CORNEAL PERFORATION ( 4 FDA reports)
CORYNEBACTERIUM INFECTION ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
CSF CULTURE POSITIVE ( 4 FDA reports)
CSF PRESSURE INCREASED ( 4 FDA reports)
CSF TEST ABNORMAL ( 4 FDA reports)
CULTURE STOOL POSITIVE ( 4 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 4 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 4 FDA reports)
DEAFNESS NEUROSENSORY ( 4 FDA reports)
DEAFNESS UNILATERAL ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 4 FDA reports)
DISSEMINATED CRYPTOCOCCOSIS ( 4 FDA reports)
DRUG CLEARANCE DECREASED ( 4 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 4 FDA reports)
EMPYEMA ( 4 FDA reports)
ENDOCARDITIS BACTERIAL ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
EYE EXCISION ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
GASTRITIS EROSIVE ( 4 FDA reports)
GLOMERULONEPHRITIS RAPIDLY PROGRESSIVE ( 4 FDA reports)
HAEMOPHILUS INFECTION ( 4 FDA reports)
HAEMOSIDEROSIS ( 4 FDA reports)
HALLUCINATION, AUDITORY ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HEPATOCELLULAR INJURY ( 4 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 4 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPOPNOEA ( 4 FDA reports)
HYPOPROTEINAEMIA ( 4 FDA reports)
INCREASED APPETITE ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INTRA-UTERINE DEATH ( 4 FDA reports)
KETOACIDOSIS ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
LIPASE INCREASED ( 4 FDA reports)
LOCAL SWELLING ( 4 FDA reports)
LOCALISED INFECTION ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
MYCOTIC ANEURYSM ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 4 FDA reports)
NEOPLASM PROGRESSION ( 4 FDA reports)
NEPHRITIS ( 4 FDA reports)
NEPHRITIS INTERSTITIAL ( 4 FDA reports)
NEPHROCALCINOSIS ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NOCARDIOSIS ( 4 FDA reports)
OPERATIVE HAEMORRHAGE ( 4 FDA reports)
OPPORTUNISTIC INFECTION ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
ORGAN FAILURE ( 4 FDA reports)
OTITIS MEDIA ( 4 FDA reports)
PANCREATIC NECROSIS ( 4 FDA reports)
PERFORMANCE STATUS DECREASED ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PHLEBITIS ( 4 FDA reports)
PLEOCYTOSIS ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PNEUMONIA ASPERGILLUS ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
PNEUMONIA ESCHERICHIA ( 4 FDA reports)
PNEUMONIA NECROTISING ( 4 FDA reports)
PORTAL VEIN THROMBOSIS ( 4 FDA reports)
POST TRANSPLANT LYMPHOPROLIFERATIVE DISORDER ( 4 FDA reports)
PULMONARY MASS ( 4 FDA reports)
PULMONARY TUBERCULOSIS ( 4 FDA reports)
PURULENCE ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RENAL ARTERY STENOSIS ( 4 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 4 FDA reports)
RESPIRATORY MONILIASIS ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SCEDOSPORIUM INFECTION ( 4 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 4 FDA reports)
SPLEEN DISORDER ( 4 FDA reports)
SPUTUM ABNORMAL ( 4 FDA reports)
SPUTUM DISCOLOURED ( 4 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 4 FDA reports)
SUBCUTANEOUS ABSCESS ( 4 FDA reports)
SUPERINFECTION BACTERIAL ( 4 FDA reports)
THROMBOPHLEBITIS ( 4 FDA reports)
TOXIC SHOCK SYNDROME ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
VENOUS OCCLUSION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 4 FDA reports)
VITAL CAPACITY DECREASED ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 4 FDA reports)
WOUND DEHISCENCE ( 4 FDA reports)
ABDOMINAL HERNIA ( 3 FDA reports)
ABDOMINAL INFECTION ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ABDOMINAL WALL DISORDER ( 3 FDA reports)
ABSCESS BACTERIAL ( 3 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 3 FDA reports)
ACUTE INTERSTITIAL PNEUMONITIS ( 3 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 3 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA DIFFERENTIATION SYNDROME ( 3 FDA reports)
ADRENAL CORTEX NECROSIS ( 3 FDA reports)
ADRENAL INSUFFICIENCY ( 3 FDA reports)
ALLOGENIC BONE MARROW TRANSPLANTATION THERAPY ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
AMBLYOPIA ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANGIONEUROTIC OEDEMA ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
AORTIC ANEURYSM ( 3 FDA reports)
APPENDIX DISORDER ( 3 FDA reports)
ARACHNOIDITIS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLADDER DILATATION ( 3 FDA reports)
BLOOD BILIRUBIN ABNORMAL ( 3 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CHLORIDE INCREASED ( 3 FDA reports)
BLOOD GASES ABNORMAL ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD MAGNESIUM DECREASED ( 3 FDA reports)
BLOOD PH DECREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BLOOD SODIUM INCREASED ( 3 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 3 FDA reports)
BONE NEOPLASM MALIGNANT ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
CATARACT OPERATION ( 3 FDA reports)
CATATONIA ( 3 FDA reports)
CATHETER RELATED COMPLICATION ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CELLULITIS GANGRENOUS ( 3 FDA reports)
CELLULITIS ORBITAL ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 3 FDA reports)
CHOLINERGIC SYNDROME ( 3 FDA reports)
CHORIOMENINGITIS LYMPHOCYTIC ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 3 FDA reports)
CONDUCTION DISORDER ( 3 FDA reports)
COR PULMONALE ( 3 FDA reports)
CRYPTOCOCCAL CUTANEOUS INFECTION ( 3 FDA reports)
CRYPTOCOCCUS TEST POSITIVE ( 3 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 3 FDA reports)
CYSTITIS VIRAL ( 3 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 3 FDA reports)
DECEREBRATION ( 3 FDA reports)
DERMATITIS ALLERGIC ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 3 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 3 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 3 FDA reports)
ENTEROBACTER PNEUMONIA ( 3 FDA reports)
ERYSIPELOID ( 3 FDA reports)
EXANTHEM ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
FEBRILE INFECTION ( 3 FDA reports)
FUNGAL PERITONITIS ( 3 FDA reports)
GALLBLADDER DISORDER ( 3 FDA reports)
GANGRENE ( 3 FDA reports)
GASTRIC HAEMORRHAGE ( 3 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 3 FDA reports)
GASTROINTESTINAL PAIN ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GLOMERULONEPHROPATHY ( 3 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 3 FDA reports)
GRAFT COMPLICATION ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
H1N1 INFLUENZA ( 3 FDA reports)
HAEMANGIOMA OF LIVER ( 3 FDA reports)
HAEMOGLOBINURIA ( 3 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HIATUS HERNIA ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERMETROPIA ( 3 FDA reports)
HYPHAEMA ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
HYPOTONIA ( 3 FDA reports)
IMMUNODEFICIENCY ( 3 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
INTESTINAL PROLAPSE ( 3 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 3 FDA reports)
IRON DEFICIENCY ANAEMIA ( 3 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 3 FDA reports)
LARYNGITIS BACTERIAL ( 3 FDA reports)
LARYNGITIS FUNGAL ( 3 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 3 FDA reports)
LICHENOID KERATOSIS ( 3 FDA reports)
LUNG CONSOLIDATION ( 3 FDA reports)
LYMPHANGIOLEIOMYOMATOSIS ( 3 FDA reports)
LYMPHOCELE MARSUPIALISATION ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MASS ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
MENINGEAL DISORDER ( 3 FDA reports)
MENINGITIS TUBERCULOUS ( 3 FDA reports)
METAPNEUMOVIRUS INFECTION ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
METASTASES TO LYMPH NODES ( 3 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MULTIPLE FRACTURES ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 3 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 3 FDA reports)
NASAL DISORDER ( 3 FDA reports)
NECROTISING COLITIS ( 3 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
NEONATAL RESPIRATORY FAILURE ( 3 FDA reports)
NEPHRITIC SYNDROME ( 3 FDA reports)
NEPHROGENIC ANAEMIA ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OESOPHAGEAL STENOSIS ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
OESOPHAGITIS ULCERATIVE ( 3 FDA reports)
OLIGOHYDRAMNIOS ( 3 FDA reports)
ORAL FUNGAL INFECTION ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OSTEOCHONDROSIS ( 3 FDA reports)
OSTEOMYELITIS FUNGAL ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 3 FDA reports)
PANOPHTHALMITIS ( 3 FDA reports)
PARACOCCIDIOIDES INFECTION ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 3 FDA reports)
PEARSON'S SYNDROME ( 3 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PITYRIASIS ( 3 FDA reports)
PLEURAL INFECTION BACTERIAL ( 3 FDA reports)
PNEUMATIC COMPRESSION THERAPY ( 3 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 3 FDA reports)
PNEUMONIA HERPES VIRAL ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
POLYDACTYLY ( 3 FDA reports)
POLYDIPSIA ( 3 FDA reports)
POLYP ( 3 FDA reports)
POLYURIA ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PRESCRIBED OVERDOSE ( 3 FDA reports)
PROTEIN TOTAL INCREASED ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PUNCTURE SITE INFECTION ( 3 FDA reports)
PYODERMA GANGRENOSUM ( 3 FDA reports)
PYURIA ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RENAL TUBULAR ACIDOSIS ( 3 FDA reports)
RENAL VASCULITIS ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RESPIRATORY RATE DECREASED ( 3 FDA reports)
RETINAL ISCHAEMIA ( 3 FDA reports)
RETINAL VEIN OCCLUSION ( 3 FDA reports)
RETINOIC ACID SYNDROME ( 3 FDA reports)
RIGHT VENTRICULAR DYSFUNCTION ( 3 FDA reports)
ROTATOR CUFF SYNDROME ( 3 FDA reports)
SALMONELLOSIS ( 3 FDA reports)
SEPSIS SYNDROME ( 3 FDA reports)
SEROMA ( 3 FDA reports)
SINUS BRADYCARDIA ( 3 FDA reports)
SKIN MASS ( 3 FDA reports)
SKIN TOXICITY ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 3 FDA reports)
SPINAL FRACTURE ( 3 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 3 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 3 FDA reports)
STOMATITIS NECROTISING ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
SUTURE RUPTURE ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
TENDON RUPTURE ( 3 FDA reports)
THROMBOCYTHAEMIA ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TORULOPSIS INFECTION ( 3 FDA reports)
TRACHEOSTOMY ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
URETERAL STENT INSERTION ( 3 FDA reports)
URINARY TRACT OBSTRUCTION ( 3 FDA reports)
URINE KETONE BODY PRESENT ( 3 FDA reports)
URINOMA ( 3 FDA reports)
VAGINAL CELLULITIS ( 3 FDA reports)
VEILLONELLA INFECTION ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VISUAL DISTURBANCE ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABSCESS FUNGAL ( 2 FDA reports)
ACINETOBACTER TEST POSITIVE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ADJUSTMENT DISORDER ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ALTERNARIA INFECTION ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANEURYSM ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
AORTIC ANEURYSM RUPTURE ( 2 FDA reports)
AORTIC VALVE DISEASE ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
APPENDICITIS PERFORATED ( 2 FDA reports)
APPLICATION SITE OEDEMA ( 2 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHROSCOPIC SURGERY ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASPERGILLUS TEST POSITIVE ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATRIAL TACHYCARDIA ( 2 FDA reports)
AXONAL NEUROPATHY ( 2 FDA reports)
B-CELL LYMPHOMA ( 2 FDA reports)
B-CELL SMALL LYMPHOCYTIC LYMPHOMA ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BILE DUCT STENOSIS ( 2 FDA reports)
BIOPSY BONE MARROW ABNORMAL ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BONE ABSCESS ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BONE EROSION ( 2 FDA reports)
BONE LESION ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRADYCARDIA NEONATAL ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN HYPOXIA ( 2 FDA reports)
BRAIN MASS ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
BRONCHOSTENOSIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CARCINOID TUMOUR ( 2 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 2 FDA reports)
CARPAL TUNNEL SYNDROME ( 2 FDA reports)
CARTILAGE INJURY ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETER REMOVAL ( 2 FDA reports)
CATHETER SEPSIS ( 2 FDA reports)
CELL DEATH ( 2 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CERUMEN IMPACTION ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CHOROIDITIS ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CITROBACTER SEPSIS ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COAGULATION FACTOR XIII LEVEL DECREASED ( 2 FDA reports)
COMMUNICATION DISORDER ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED LUNG ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CRANIOTOMY ( 2 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 2 FDA reports)
CREPITATIONS ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CSF WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
CULTURE POSITIVE ( 2 FDA reports)
CUTANEOUS LEISHMANIASIS ( 2 FDA reports)
CYTOMEGALOVIRUS GASTRITIS ( 2 FDA reports)
CYTOMEGALOVIRUS GASTROENTERITIS ( 2 FDA reports)
DACRYOCANALICULITIS ( 2 FDA reports)
DEAFNESS BILATERAL ( 2 FDA reports)
DEBRIDEMENT ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DEVICE FAILURE ( 2 FDA reports)
DEVICE OCCLUSION ( 2 FDA reports)
DIABETIC HYPEROSMOLAR COMA ( 2 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DISSEMINATED CYTOMEGALOVIRAL INFECTION ( 2 FDA reports)
DISSEMINATED TUBERCULOSIS ( 2 FDA reports)
DRUG TOLERANCE ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSPHASIA ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 2 FDA reports)
EMPTY SELLA SYNDROME ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENDOSCOPIC ULTRASOUND ABNORMAL ( 2 FDA reports)
ENTERITIS INFECTIOUS ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
EUTHYROID SICK SYNDROME ( 2 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 2 FDA reports)
EXTRASKELETAL OSSIFICATION ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EYE ABSCESS ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FLUID IMBALANCE ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FOETAL GROWTH RESTRICTION ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
FUNGAL OESOPHAGITIS ( 2 FDA reports)
FUNGUS STOOL IDENTIFIED ( 2 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 2 FDA reports)
GASTROENTERITIS SALMONELLA ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL MUCOSAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLOSSECTOMY ( 2 FDA reports)
HAEMOPHILUS TEST POSITIVE ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HAEMORRHAGIC INFARCTION ( 2 FDA reports)
HAEMORRHOIDS ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATIC ARTERY ANEURYSM ( 2 FDA reports)
HEPATIC CONGESTION ( 2 FDA reports)
HEPATIC FIBROSIS ( 2 FDA reports)
HERNIA ( 2 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 2 FDA reports)
HODGKIN'S DISEASE NODULAR SCLEROSIS STAGE IV ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
ILEAL PERFORATION ( 2 FDA reports)
IMPATIENCE ( 2 FDA reports)
IMPLANT SITE INFECTION ( 2 FDA reports)
INFARCTION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
IUCD COMPLICATION ( 2 FDA reports)
KERATITIS ( 2 FDA reports)
KERATITIS HERPETIC ( 2 FDA reports)
KIDNEY INFECTION ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LACTOBACILLUS INFECTION ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LAPAROTOMY ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEFT VENTRICULAR FAILURE ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LEUKAEMIA PLASMACYTIC ( 2 FDA reports)
LEUKAEMIC INFILTRATION EXTRAMEDULLARY ( 2 FDA reports)
LEUKOPLAKIA ORAL ( 2 FDA reports)
LICHENIFICATION ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
LUNG LOBECTOMY ( 2 FDA reports)
LUNG TRANSPLANT ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MAGNESIUM DEFICIENCY ( 2 FDA reports)
MANIA ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
MEDICAL DEVICE DISCOMFORT ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO MENINGES ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
METHYLOBACTERIUM INFECTION ( 2 FDA reports)
MICROANGIOPATHY ( 2 FDA reports)
MITRAL VALVE REPAIR ( 2 FDA reports)
MOLLUSCUM CONTAGIOSUM ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYELITIS ( 2 FDA reports)
MYOPATHY ( 2 FDA reports)
NASAL ULCER ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEONATAL CARDIAC FAILURE ( 2 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 2 FDA reports)
NEPHROSCLEROSIS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 2 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
NOROVIRUS TEST POSITIVE ( 2 FDA reports)
OCULOGYRIC CRISIS ( 2 FDA reports)
OESOPHAGEAL CARCINOMA ( 2 FDA reports)
OESOPHAGEAL INFECTION ( 2 FDA reports)
OESOPHAGEAL OBSTRUCTION ( 2 FDA reports)
OPTIC NERVE INJURY ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
OPTIC NEUROPATHY ( 2 FDA reports)
ORAL DISORDER ( 2 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OROPHARYNGEAL CANDIDIASIS ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PANIC DISORDER ( 2 FDA reports)
PARASITE DNA TEST POSITIVE ( 2 FDA reports)
PAROTID ABSCESS ( 2 FDA reports)
PAROTITIS ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERITONITIS SCLEROSING ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLEURAL INFECTION ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLYPECTOMY ( 2 FDA reports)
POLYSEROSITIS ( 2 FDA reports)
PORPHYRIA ACUTE ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
PROCEDURAL SITE REACTION ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY CAVITATION ( 2 FDA reports)
PULMONARY TOXICITY ( 2 FDA reports)
PULMONARY VASCULITIS ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RECTAL PERFORATION ( 2 FDA reports)
RECURRENT CANCER ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL ABSCESS ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RENAL NECROSIS ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS TEST POSITIVE ( 2 FDA reports)
RETINAL HAEMORRHAGE ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
SCAR ( 2 FDA reports)
SCOTOMA ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SKIN DESQUAMATION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN NECROSIS ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SOFT TISSUE INFECTION ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SPLEEN CONGESTION ( 2 FDA reports)
STAPHYLOCOCCAL SCALDED SKIN SYNDROME ( 2 FDA reports)
STEROID THERAPY ( 2 FDA reports)
STILL'S DISEASE ADULT ONSET ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
SURGICAL PROCEDURE REPEATED ( 2 FDA reports)
SWEAT GLAND DISORDER ( 2 FDA reports)
SWELLING ( 2 FDA reports)
THORACIC CAVITY DRAINAGE ( 2 FDA reports)
THORACOTOMY ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYROID CYST ( 2 FDA reports)
TONGUE COATED ( 2 FDA reports)
TONGUE NECROSIS ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 2 FDA reports)
TRACHEAL ULCER ( 2 FDA reports)
TRANSVERSE SINUS THROMBOSIS ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 2 FDA reports)
URETERAL NECROSIS ( 2 FDA reports)
URETERAL STENT REMOVAL ( 2 FDA reports)
URETERIC DILATATION ( 2 FDA reports)
URETERIC OBSTRUCTION ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
UVEITIS ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VANISHING BILE DUCT SYNDROME ( 2 FDA reports)
VASCULAR PSEUDOANEURYSM RUPTURED ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR FAILURE ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VESICAL FISTULA ( 2 FDA reports)
VIRUS URINE TEST POSITIVE ( 2 FDA reports)
VITAMIN B12 ABNORMAL ( 2 FDA reports)
WOUND DECOMPOSITION ( 2 FDA reports)
ABDOMINAL ADHESIONS ( 1 FDA reports)
ABDOMINAL COMPARTMENT SYNDROME ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS DRAINAGE ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACINETOBACTER BACTERAEMIA ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACQUIRED EPIDERMOLYSIS BULLOSA ( 1 FDA reports)
ACTINOMYCOSIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE PULMONARY HISTOPLASMOSIS ( 1 FDA reports)
ADENOVIRAL HAEMORRHAGIC CYSTITIS ( 1 FDA reports)
ADENOVIRUS TEST POSITIVE ( 1 FDA reports)
ADRENAL ADENOMA ( 1 FDA reports)
ADRENOCORTICAL INSUFFICIENCY CHRONIC ( 1 FDA reports)
ADULT T-CELL LYMPHOMA/LEUKAEMIA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AIDS RELATED COMPLEX ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
ALVEOLAR PROTEINOSIS ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAEMIA MEGALOBLASTIC ( 1 FDA reports)
ANAEMIA NEONATAL ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANAL ABSCESS ( 1 FDA reports)
ANAL FUNGAL INFECTION ( 1 FDA reports)
ANAL SKIN TAGS ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANASTOMOTIC ULCER PERFORATION ( 1 FDA reports)
ANEURYSM REPAIR ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANION GAP INCREASED ( 1 FDA reports)
ANORECTAL INFECTION ( 1 FDA reports)
ANTERIOR CHAMBER FIBRIN ( 1 FDA reports)
ANTHRAX ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIBIOTIC LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC RUPTURE ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE STENOSIS ( 1 FDA reports)
APGAR SCORE LOW ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APOPTOSIS ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
ARTERITIS INFECTIVE ( 1 FDA reports)
ARTHRITIS FUNGAL ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
ASYMPTOMATIC BACTERIURIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIA SPUTUM IDENTIFIED ( 1 FDA reports)
BACTEROIDES INFECTION ( 1 FDA reports)
BAND NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
BASE EXCESS DECREASED ( 1 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BILOMA ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER PAIN ( 1 FDA reports)
BLADDER SPASM ( 1 FDA reports)
BLAST CELL COUNT INCREASED ( 1 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 1 FDA reports)
BLASTOMYCOSIS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ABNORMAL ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE DECREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CALCITONIN DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD ERYTHROPOIETIN INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM INCREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE INFARCTION ( 1 FDA reports)
BONE SARCOMA ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BRAIN STEM AUDITORY EVOKED RESPONSE ABNORMAL ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL ANASTOMOSIS ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ALLERGIC ( 1 FDA reports)
BUCCAL POLYP ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CALCIUM IONISED DECREASED ( 1 FDA reports)
CANDIDA OSTEOMYELITIS ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CANDIDURIA ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC FUNCTION TEST ABNORMAL ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC OUTPUT ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETERISATION CARDIAC ( 1 FDA reports)
CAUDA EQUINA SYNDROME ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM NEOPLASM ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR ATROPHY ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CERVICAL CORD COMPRESSION ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CHEST EXPANSION DECREASED ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHORIORETINITIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CNS VENTRICULITIS ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COCHLEA IMPLANT ( 1 FDA reports)
COLITIS PSEUDOMEMBRANOUS ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLOUR BLINDNESS ACQUIRED ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF TRANSPLANTED HEART ( 1 FDA reports)
COMPUTERISED TOMOGRAM THORAX ABNORMAL ( 1 FDA reports)
CONGENITAL CYSTIC KIDNEY DISEASE ( 1 FDA reports)
CONJUNCTIVAL DISORDER ( 1 FDA reports)
CONJUNCTIVITIS VIRAL ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CRACKLES LUNG ( 1 FDA reports)
CRITICAL ILLNESS POLYNEUROPATHY ( 1 FDA reports)
CRYING ( 1 FDA reports)
CSF GLUCOSE DECREASED ( 1 FDA reports)
CSF GLUCOSE INCREASED ( 1 FDA reports)
CULTURE THROAT POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYP2C19 POLYMORPHISM ( 1 FDA reports)
CYSTOID MACULAR OEDEMA ( 1 FDA reports)
CYTOMEGALOVIRUS ENTEROCOLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS GASTROINTESTINAL INFECTION ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
CYTOTOXIC OEDEMA ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DENTAL OPERATION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMATITIS EXFOLIATIVE GENERALISED ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISORDER OF ORBIT ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG INTERACTION INHIBITION ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG WITHDRAWAL CONVULSIONS ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
ECG SIGNS OF MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
ECHOCARDIOGRAM ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECHOLALIA ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENCEPHALITIS FUNGAL ( 1 FDA reports)
ENCEPHALITIS MENINGOCOCCAL ( 1 FDA reports)
ENCEPHALITIS PROTOZOAL ( 1 FDA reports)
ENCEPHALOMALACIA ( 1 FDA reports)
ENDOCARDIAL DISEASE ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROBIASIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPHELIDES ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPSTEIN-BARR VIRAEMIA ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EUBACTERIUM INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXOPHTHALMOS ( 1 FDA reports)
EXTRADURAL HAEMATOMA ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE COMPLICATION ASSOCIATED WITH DEVICE ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FAT NECROSIS ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEMORAL NECK FRACTURE ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FISTULA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOD ALLERGY ( 1 FDA reports)
FORCED EXPIRATORY VOLUME DECREASED ( 1 FDA reports)
FOREIGN BODY TRAUMA ( 1 FDA reports)
FREE HAEMOGLOBIN PRESENT ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
FUNDOSCOPY ABNORMAL ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
GALLBLADDER OEDEMA ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS ROTAVIRUS ( 1 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL NECROSIS ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GIARDIASIS ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLIOBLASTOMA MULTIFORME ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULAR VASCULAR DISORDER ( 1 FDA reports)
GLOMERULOSCLEROSIS ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLUTAMATE DEHYDROGENASE INCREASED ( 1 FDA reports)
GLYCOPEPTIDE ANTIBIOTIC RESISTANT ENTEROCOCCAL INFECTION ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GRUNTING ( 1 FDA reports)
HAEMATOLOGICAL MALIGNANCY ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HAEMOGLOBIN S DECREASED ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEART TRANSPLANT REJECTION ( 1 FDA reports)
HEAT ILLNESS ( 1 FDA reports)
HEMIANOPIA HOMONYMOUS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ARTERY STENOSIS ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC INFECTION ( 1 FDA reports)
HEPATIC INFECTION FUNGAL ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATITIS B SURFACE ANTIGEN POSITIVE ( 1 FDA reports)
HEPATITIS GRANULOMATOUS ( 1 FDA reports)
HEPATO-LENTICULAR DEGENERATION ( 1 FDA reports)
HEPATOBILIARY NEOPLASM ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HEPATORENAL SYNDROME ( 1 FDA reports)
HEPATOSPLENOMEGALY NEONATAL ( 1 FDA reports)
HERNIA OBSTRUCTIVE ( 1 FDA reports)
HERPES OESOPHAGITIS ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HUMAN POLYOMAVIRUS INFECTION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERREFLEXIA ( 1 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTROPHIC CARDIOMYOPATHY ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOCHROMIC ANAEMIA ( 1 FDA reports)
HYPOGONADISM ( 1 FDA reports)
HYPOSTHENURIA ( 1 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEITIS ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 1 FDA reports)
IMPAIRED SELF-CARE ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCISION SITE ABSCESS ( 1 FDA reports)
INCISION SITE HAEMATOMA ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION MASKED ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFECTIVE THROMBOSIS ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INGUINAL MASS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE WARMTH ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERSTITIAL GRANULOMATOUS DERMATITIS ( 1 FDA reports)
INTESTINAL ULCER ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRIDOCYCLITIS ( 1 FDA reports)
IVTH NERVE PARALYSIS ( 1 FDA reports)
JAUNDICE NEONATAL ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KERATITIS BACTERIAL ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KLEBSIELLA BACTERAEMIA ( 1 FDA reports)
KLEBSIELLA SEPSIS ( 1 FDA reports)
KYPHOSIS ( 1 FDA reports)
LABILE BLOOD PRESSURE ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LEISHMANIASIS ( 1 FDA reports)
LENTIGO ( 1 FDA reports)
LEUKODYSTROPHY ( 1 FDA reports)
LINEAR IGA DISEASE ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP INFECTION ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER OPERATION ( 1 FDA reports)
LIVER PALPABLE SUBCOSTAL ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG HERNIA ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACROCYTOSIS ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MALARIA ( 1 FDA reports)
MALIGNANT FIBROUS HISTIOCYTOMA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDULLOBLASTOMA RECURRENT ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS CHEMICAL ( 1 FDA reports)
MENINGITIS COCCIDIOIDES ( 1 FDA reports)
MENINGITIS FUNGAL ( 1 FDA reports)
MENINGITIS STAPHYLOCOCCAL ( 1 FDA reports)
METAPLASIA ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MONOCYTOSIS ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUCOCUTANEOUS CANDIDIASIS ( 1 FDA reports)
MUCOPOLYSACCHARIDOSIS VI ( 1 FDA reports)
MUCOSAL INFECTION ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE OPERATION ( 1 FDA reports)
MYCETOMA MYCOTIC ( 1 FDA reports)
MYCOBACTERIUM TEST POSITIVE ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
MYELOPATHY ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NATURAL KILLER T CELL COUNT INCREASED ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NECROTISING SCLERITIS ( 1 FDA reports)
NEONATAL CANDIDA INFECTION ( 1 FDA reports)
NEONATAL HEPATOMEGALY ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM RECURRENCE ( 1 FDA reports)
NEOVASCULARISATION ( 1 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NEURODEGENERATIVE DISORDER ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
NORMAL PRESSURE HYDROCEPHALUS ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCULAR DISCOMFORT ( 1 FDA reports)
OPTIC DISC HYPERAEMIA ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
ORTHOPEDIC PROCEDURE ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ACUTE ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OSTEOPOROTIC FRACTURE ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC HAEMORRHAGE ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAPILLARY MUSCLE RUPTURE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARALYSIS FLACCID ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARVOVIRUS INFECTION ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEAU D'ORANGE ( 1 FDA reports)
PEDAL PULSE ABSENT ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PENICILLIOSIS ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERFORATED ULCER ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERITONEAL DIALYSIS ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HERNIA ( 1 FDA reports)
PERITONSILLAR ABSCESS ( 1 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 1 FDA reports)
PH BODY FLUID DECREASED ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHONOPHOBIA ( 1 FDA reports)
PHOTODERMATOSIS ( 1 FDA reports)
PIGMENTED NAEVUS ( 1 FDA reports)
PITUITARY INFARCTION ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOCEPHALUS ( 1 FDA reports)
PNEUMOCONIOSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA ADENOVIRAL ( 1 FDA reports)
PNEUMONIA CHLAMYDIAL ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
PNEUMONIA RESPIRATORY SYNCYTIAL VIRAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
POLYCHROMASIA ( 1 FDA reports)
POLYNEUROPATHY CHRONIC ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
POSITIVE ROMBERGISM ( 1 FDA reports)
POSTOPERATIVE ADHESION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRECURSOR T-LYMPHOBLASTIC LYMPHOMA/LEUKAEMIA RECURRENT ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMEDICATION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROTHROMBIN LEVEL ABNORMAL ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOTIC DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 1 FDA reports)
PULMONARY FUNCTION TEST ABNORMAL ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY PERCUSSION TEST ABNORMALITY ( 1 FDA reports)
PULMONARY SEPSIS ( 1 FDA reports)
PULMONARY VENO-OCCLUSIVE DISEASE ( 1 FDA reports)
PUPILLARY DISORDER ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
QRS AXIS ABNORMAL ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RADIATION INJURY ( 1 FDA reports)
RADIATION INTERACTION ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
RELAPSING FEVER ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL ISCHAEMIA ( 1 FDA reports)
RENAL LYMPHOCELE ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
REPETITIVE SPEECH ( 1 FDA reports)
RESIDUAL URINE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DISORDER NEONATAL ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETICULOCYTE COUNT DECREASED ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL INFARCTION ( 1 FDA reports)
RETINAL INFILTRATES ( 1 FDA reports)
RETINAL INJURY ( 1 FDA reports)
RETINAL OEDEMA ( 1 FDA reports)
RETINAL TOXICITY ( 1 FDA reports)
RETINAL VASCULAR DISORDER ( 1 FDA reports)
RETINOPATHY OF PREMATURITY ( 1 FDA reports)
RHEUMATOID VASCULITIS ( 1 FDA reports)
RHINOVIRUS INFECTION ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SCLERAL DISORDER ( 1 FDA reports)
SCLERAL HAEMORRHAGE ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SCROTAL ULCER ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSORIMOTOR DISORDER ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERRATIA TEST POSITIVE ( 1 FDA reports)
SHORT-BOWEL SYNDROME ( 1 FDA reports)
SICCA SYNDROME ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN HYPERTROPHY ( 1 FDA reports)
SKIN HYPOPIGMENTATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SMALL INTESTINE GANGRENE ( 1 FDA reports)
SOLAR ELASTOSIS ( 1 FDA reports)
SOMNOLENCE NEONATAL ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 1 FDA reports)
SPINAL PAIN ( 1 FDA reports)
SPINOCEREBELLAR DISORDER ( 1 FDA reports)
SPLENECTOMY ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STENT REMOVAL ( 1 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 1 FDA reports)
STRESS ULCER ( 1 FDA reports)
SUBCUTANEOUS EMPHYSEMA ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS RASH ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC PROCEDURE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPY CESSATION ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOTIC STROKE ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
THYROIDITIS ACUTE ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC SHOCK SYNDROME STAPHYLOCOCCAL ( 1 FDA reports)
TOXOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
TRACHEAL HAEMORRHAGE ( 1 FDA reports)
TRACHEAL INJURY ( 1 FDA reports)
TRACHEAL STENOSIS ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUMOUR HAEMORRHAGE ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNEMPLOYMENT ( 1 FDA reports)
URETERAL DISORDER ( 1 FDA reports)
URETHRAL HAEMORRHAGE ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URTICARIA PIGMENTOSA ( 1 FDA reports)
UTERINE DISORDER ( 1 FDA reports)
VAGINAL CANDIDIASIS ( 1 FDA reports)
VAGINAL DISORDER ( 1 FDA reports)
VAGINAL LESION ( 1 FDA reports)
VARICELLA ( 1 FDA reports)
VARICELLA VIRUS TEST POSITIVE ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VEILLONELLA TEST POSITIVE ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VERTICAL INFECTION TRANSMISSION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VIRAL MUTATION IDENTIFIED ( 1 FDA reports)
VIRAL UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
VITAMIN B12 INCREASED ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS HAEMORRHAGE ( 1 FDA reports)
VITREOUS OPACITIES ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOCAL CORD PARESIS ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WEGENER'S GRANULOMATOSIS ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND INFECTION BACTERIAL ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
WOUND TREATMENT ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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