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

PYREXIA ( 186 FDA reports)
SEPSIS ( 143 FDA reports)
RENAL FAILURE ACUTE ( 134 FDA reports)
RENAL FAILURE ( 125 FDA reports)
THROMBOCYTOPENIA ( 123 FDA reports)
PNEUMONIA ( 112 FDA reports)
SEPTIC SHOCK ( 112 FDA reports)
HYPOTENSION ( 102 FDA reports)
DIARRHOEA ( 95 FDA reports)
NEUTROPENIA ( 95 FDA reports)
FEBRILE NEUTROPENIA ( 89 FDA reports)
DRUG INEFFECTIVE ( 88 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 87 FDA reports)
DYSPNOEA ( 87 FDA reports)
MULTI-ORGAN FAILURE ( 85 FDA reports)
ANAEMIA ( 83 FDA reports)
DRUG INTERACTION ( 82 FDA reports)
PANCYTOPENIA ( 82 FDA reports)
VOMITING ( 80 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 69 FDA reports)
ABDOMINAL PAIN ( 64 FDA reports)
CONVULSION ( 62 FDA reports)
TACHYCARDIA ( 57 FDA reports)
CONDITION AGGRAVATED ( 56 FDA reports)
DEATH ( 55 FDA reports)
HAEMOGLOBIN DECREASED ( 55 FDA reports)
NAUSEA ( 54 FDA reports)
BLOOD BILIRUBIN INCREASED ( 53 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 53 FDA reports)
PLATELET COUNT DECREASED ( 52 FDA reports)
HYPOKALAEMIA ( 49 FDA reports)
RESPIRATORY DISTRESS ( 49 FDA reports)
HEPATIC FAILURE ( 48 FDA reports)
LEUKOPENIA ( 48 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 46 FDA reports)
RASH ( 46 FDA reports)
CYTOLYTIC HEPATITIS ( 45 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 45 FDA reports)
HYPERKALAEMIA ( 45 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 45 FDA reports)
PLEURAL EFFUSION ( 44 FDA reports)
RESPIRATORY FAILURE ( 43 FDA reports)
ABDOMINAL PAIN UPPER ( 42 FDA reports)
PAIN ( 42 FDA reports)
BLOOD CREATININE INCREASED ( 41 FDA reports)
CHOLESTASIS ( 41 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 41 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 40 FDA reports)
PSEUDOMONAS INFECTION ( 40 FDA reports)
RENAL IMPAIRMENT ( 39 FDA reports)
BRADYCARDIA ( 37 FDA reports)
STAPHYLOCOCCAL INFECTION ( 37 FDA reports)
DRUG TOXICITY ( 36 FDA reports)
ERYTHEMA ( 36 FDA reports)
HYPOGLYCAEMIA ( 36 FDA reports)
INFECTION ( 36 FDA reports)
COMA ( 35 FDA reports)
HAEMATURIA ( 35 FDA reports)
ARRHYTHMIA ( 34 FDA reports)
DEHYDRATION ( 33 FDA reports)
HEPATOTOXICITY ( 33 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 32 FDA reports)
BLOOD UREA INCREASED ( 32 FDA reports)
CARDIAC ARREST ( 32 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 32 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 32 FDA reports)
HYPERTENSION ( 32 FDA reports)
JAUNDICE ( 31 FDA reports)
METABOLIC ACIDOSIS ( 31 FDA reports)
PANCREATITIS ( 31 FDA reports)
AGRANULOCYTOSIS ( 30 FDA reports)
BACTERIAL INFECTION ( 30 FDA reports)
BONE MARROW FAILURE ( 30 FDA reports)
OEDEMA PERIPHERAL ( 30 FDA reports)
PERICARDIAL EFFUSION ( 30 FDA reports)
PRURITUS ( 30 FDA reports)
RASH MACULO-PAPULAR ( 30 FDA reports)
DERMATITIS EXFOLIATIVE ( 29 FDA reports)
ENCEPHALOPATHY ( 29 FDA reports)
LYMPHADENOPATHY ( 28 FDA reports)
VISUAL ACUITY REDUCED ( 28 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 27 FDA reports)
COUGH ( 27 FDA reports)
CYANOSIS ( 27 FDA reports)
EPISTAXIS ( 27 FDA reports)
MUCOSAL INFLAMMATION ( 27 FDA reports)
NEPHROPATHY TOXIC ( 27 FDA reports)
PULMONARY HYPERTENSION ( 27 FDA reports)
ABDOMINAL DISTENSION ( 26 FDA reports)
ATRIAL FIBRILLATION ( 26 FDA reports)
HYPERBILIRUBINAEMIA ( 26 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 26 FDA reports)
OVERDOSE ( 26 FDA reports)
RENAL TUBULAR NECROSIS ( 26 FDA reports)
CANDIDIASIS ( 25 FDA reports)
DYSPEPSIA ( 25 FDA reports)
HYPERGLYCAEMIA ( 25 FDA reports)
NEONATAL DISORDER ( 25 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 25 FDA reports)
TOXIC SKIN ERUPTION ( 25 FDA reports)
URINARY TRACT INFECTION ( 25 FDA reports)
ANURIA ( 24 FDA reports)
CARDIO-RESPIRATORY ARREST ( 24 FDA reports)
CONFUSIONAL STATE ( 24 FDA reports)
ELECTROLYTE IMBALANCE ( 24 FDA reports)
HAEMORRHAGE ( 24 FDA reports)
SKIN EXFOLIATION ( 24 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 23 FDA reports)
ASTHENIA ( 23 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 23 FDA reports)
HAEMATOCRIT DECREASED ( 23 FDA reports)
HEADACHE ( 23 FDA reports)
HYPONATRAEMIA ( 23 FDA reports)
LACTIC ACIDOSIS ( 23 FDA reports)
PERITONITIS ( 23 FDA reports)
ANXIETY ( 22 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 22 FDA reports)
DISEASE PROGRESSION ( 22 FDA reports)
EOSINOPHILIA ( 22 FDA reports)
HEPATIC ENZYME INCREASED ( 22 FDA reports)
LIVER DISORDER ( 22 FDA reports)
RENAL TUBULAR DISORDER ( 22 FDA reports)
RESPIRATORY ARREST ( 22 FDA reports)
TRANSAMINASES INCREASED ( 22 FDA reports)
BACTERAEMIA ( 21 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 21 FDA reports)
HYPOTHYROIDISM ( 21 FDA reports)
OXYGEN SATURATION DECREASED ( 21 FDA reports)
ASPERGILLOSIS ( 20 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 20 FDA reports)
COLITIS ( 20 FDA reports)
CONSTIPATION ( 20 FDA reports)
DEAFNESS ( 20 FDA reports)
FEBRILE BONE MARROW APLASIA ( 20 FDA reports)
HAEMODIALYSIS ( 20 FDA reports)
HYPERHIDROSIS ( 20 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 20 FDA reports)
MELAENA ( 20 FDA reports)
MENTAL STATUS CHANGES ( 20 FDA reports)
OEDEMA ( 20 FDA reports)
PERICARDITIS TUBERCULOUS ( 20 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 20 FDA reports)
SUDDEN DEATH ( 20 FDA reports)
ASCITES ( 19 FDA reports)
CHILLS ( 19 FDA reports)
LUNG DISORDER ( 19 FDA reports)
MEDICATION ERROR ( 19 FDA reports)
PALLOR ( 19 FDA reports)
TREMOR ( 19 FDA reports)
ACUTE PULMONARY OEDEMA ( 18 FDA reports)
COAGULOPATHY ( 18 FDA reports)
DEAFNESS NEUROSENSORY ( 18 FDA reports)
HEPATITIS ( 18 FDA reports)
LEUKOCYTOSIS ( 18 FDA reports)
MALAISE ( 18 FDA reports)
NO THERAPEUTIC RESPONSE ( 18 FDA reports)
PULMONARY OEDEMA ( 18 FDA reports)
AGITATION ( 17 FDA reports)
BLOOD CULTURE POSITIVE ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 17 FDA reports)
FLUID OVERLOAD ( 17 FDA reports)
NEUROPATHY ( 17 FDA reports)
PANCREATITIS ACUTE ( 17 FDA reports)
PNEUMATOSIS INTESTINALIS ( 17 FDA reports)
RECTAL HAEMORRHAGE ( 17 FDA reports)
STEVENS-JOHNSON SYNDROME ( 17 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 17 FDA reports)
ACIDOSIS ( 16 FDA reports)
ATELECTASIS ( 16 FDA reports)
BLOOD ALBUMIN DECREASED ( 16 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 16 FDA reports)
BRONCHOPNEUMONIA ( 16 FDA reports)
CARDIAC FAILURE ( 16 FDA reports)
CEREBRAL HAEMORRHAGE ( 16 FDA reports)
DECREASED APPETITE ( 16 FDA reports)
DIALYSIS ( 16 FDA reports)
FACE OEDEMA ( 16 FDA reports)
HAEMATEMESIS ( 16 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 16 FDA reports)
HYPOXIA ( 16 FDA reports)
NEUTROPHIL COUNT DECREASED ( 16 FDA reports)
PREMATURE BABY ( 16 FDA reports)
SINUSITIS ( 16 FDA reports)
WEIGHT DECREASED ( 16 FDA reports)
CHEILITIS ( 15 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 15 FDA reports)
HAEMOLYTIC ANAEMIA ( 15 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 15 FDA reports)
HYPERNATRAEMIA ( 15 FDA reports)
INFLAMMATION ( 15 FDA reports)
LUNG INFECTION ( 15 FDA reports)
PULMONARY HAEMORRHAGE ( 15 FDA reports)
VENTRICULAR TACHYCARDIA ( 15 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 14 FDA reports)
HAEMOPTYSIS ( 14 FDA reports)
INTESTINAL PERFORATION ( 14 FDA reports)
JAUNDICE CHOLESTATIC ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
OLIGURIA ( 14 FDA reports)
PNEUMOTHORAX ( 14 FDA reports)
PROTEINURIA ( 14 FDA reports)
PURPURA ( 14 FDA reports)
RHABDOMYOLYSIS ( 14 FDA reports)
SOMNOLENCE ( 14 FDA reports)
STATUS EPILEPTICUS ( 14 FDA reports)
BLOOD PRESSURE DECREASED ( 13 FDA reports)
BURNING SENSATION ( 13 FDA reports)
CARDIOGENIC SHOCK ( 13 FDA reports)
DRUG ERUPTION ( 13 FDA reports)
GRAND MAL CONVULSION ( 13 FDA reports)
INTERSTITIAL LUNG DISEASE ( 13 FDA reports)
MYDRIASIS ( 13 FDA reports)
MYOCLONUS ( 13 FDA reports)
NECROTISING ENTEROCOLITIS NEONATAL ( 13 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 13 FDA reports)
PAIN IN EXTREMITY ( 13 FDA reports)
PROTHROMBIN TIME PROLONGED ( 13 FDA reports)
SHOCK ( 13 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 12 FDA reports)
ACUTE RESPIRATORY FAILURE ( 12 FDA reports)
APLASIA ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 12 FDA reports)
CHEST PAIN ( 12 FDA reports)
DEPRESSION ( 12 FDA reports)
HEART RATE INCREASED ( 12 FDA reports)
HEPATOSPLENOMEGALY ( 12 FDA reports)
HYPERTENSIVE HEART DISEASE ( 12 FDA reports)
HYPERTHERMIA ( 12 FDA reports)
INFUSION RELATED REACTION ( 12 FDA reports)
LABORATORY TEST ABNORMAL ( 12 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 12 FDA reports)
MOUTH HAEMORRHAGE ( 12 FDA reports)
PATHOGEN RESISTANCE ( 12 FDA reports)
TUBERCULOSIS ( 12 FDA reports)
ABSCESS ( 11 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 11 FDA reports)
ANAL ULCER ( 11 FDA reports)
BLAST CELL CRISIS ( 11 FDA reports)
BLOOD CREATINE INCREASED ( 11 FDA reports)
BLOOD POTASSIUM INCREASED ( 11 FDA reports)
BLOOD SODIUM DECREASED ( 11 FDA reports)
BRONCHOSPASM ( 11 FDA reports)
CULTURE URINE POSITIVE ( 11 FDA reports)
DISORIENTATION ( 11 FDA reports)
ENTEROCOCCAL INFECTION ( 11 FDA reports)
HEPATOSPLENIC CANDIDIASIS ( 11 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE NEONATAL ( 11 FDA reports)
MYOCARDIAL INFARCTION ( 11 FDA reports)
ORAL HERPES ( 11 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 11 FDA reports)
UNEVALUABLE EVENT ( 11 FDA reports)
WEIGHT INCREASED ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
BLINDNESS ( 10 FDA reports)
CARDIOPULMONARY FAILURE ( 10 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
DRUG LEVEL DECREASED ( 10 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 10 FDA reports)
FLUID RETENTION ( 10 FDA reports)
FUNGAL INFECTION ( 10 FDA reports)
GASTROINTESTINAL DISORDER ( 10 FDA reports)
HYPOACUSIS ( 10 FDA reports)
LEG AMPUTATION ( 10 FDA reports)
NECROSIS ( 10 FDA reports)
NECROTISING COLITIS ( 10 FDA reports)
PERITONITIS BACTERIAL ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 10 FDA reports)
RESPIRATORY DISORDER ( 10 FDA reports)
SEPSIS NEONATAL ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
SPLENOMEGALY ( 10 FDA reports)
THROMBOSIS ( 10 FDA reports)
ARTHRALGIA ( 9 FDA reports)
BACTERIAL SEPSIS ( 9 FDA reports)
BK VIRUS INFECTION ( 9 FDA reports)
BODY TEMPERATURE INCREASED ( 9 FDA reports)
BRAIN OEDEMA ( 9 FDA reports)
CAECITIS ( 9 FDA reports)
CAPILLARY LEAK SYNDROME ( 9 FDA reports)
CARDIAC DISORDER ( 9 FDA reports)
CARDIOMYOPATHY ( 9 FDA reports)
CEREBRAL ISCHAEMIA ( 9 FDA reports)
DRUG RESISTANCE ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
HAEMODYNAMIC INSTABILITY ( 9 FDA reports)
HYPOALBUMINAEMIA ( 9 FDA reports)
HYPOVOLAEMIC SHOCK ( 9 FDA reports)
ILEUS ( 9 FDA reports)
INJURY ( 9 FDA reports)
KLEBSIELLA INFECTION ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
MYCOBACTERIAL INFECTION ( 9 FDA reports)
NEPHROTIC SYNDROME ( 9 FDA reports)
NERVOUS SYSTEM DISORDER ( 9 FDA reports)
NO ADVERSE EVENT ( 9 FDA reports)
OTOTOXICITY ( 9 FDA reports)
PANCREATITIS NECROTISING ( 9 FDA reports)
POST PROCEDURAL COMPLICATION ( 9 FDA reports)
RASH ERYTHEMATOUS ( 9 FDA reports)
RESPIRATORY RATE INCREASED ( 9 FDA reports)
SERUM SICKNESS ( 9 FDA reports)
VENTRICULAR FIBRILLATION ( 9 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
ALOPECIA ( 8 FDA reports)
ANHEDONIA ( 8 FDA reports)
ANOREXIA ( 8 FDA reports)
CARDIOMEGALY ( 8 FDA reports)
CEREBROVASCULAR ACCIDENT ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
DRUG LEVEL INCREASED ( 8 FDA reports)
ERYTHEMA MULTIFORME ( 8 FDA reports)
FEAR ( 8 FDA reports)
GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 8 FDA reports)
HEPATIC MASS ( 8 FDA reports)
HEPATIC NEOPLASM ( 8 FDA reports)
HEPATIC STEATOSIS ( 8 FDA reports)
HEPATITIS CHOLESTATIC ( 8 FDA reports)
HEPATOMEGALY ( 8 FDA reports)
HYDROCEPHALUS ( 8 FDA reports)
HYPERPYREXIA ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
MECHANICAL VENTILATION ( 8 FDA reports)
MUSCLE SPASMS ( 8 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 8 FDA reports)
PLEURISY ( 8 FDA reports)
PNEUMONIA KLEBSIELLA ( 8 FDA reports)
SKIN DISCOLOURATION ( 8 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
TUMOUR LYSIS SYNDROME ( 8 FDA reports)
URTICARIA ( 8 FDA reports)
WEGENER'S GRANULOMATOSIS ( 8 FDA reports)
ACINETOBACTER INFECTION ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
ASPARTATE AMINOTRANSFERASE ABNORMAL ( 7 FDA reports)
BACK PAIN ( 7 FDA reports)
BLISTER ( 7 FDA reports)
BONE MARROW DEPRESSION ( 7 FDA reports)
CANDIDA SEPSIS ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 7 FDA reports)
DEATH NEONATAL ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
EOSINOPHIL COUNT INCREASED ( 7 FDA reports)
ESCHERICHIA INFECTION ( 7 FDA reports)
FALL ( 7 FDA reports)
FATIGUE ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
INTENTIONAL DRUG MISUSE ( 7 FDA reports)
JAUNDICE NEONATAL ( 7 FDA reports)
LETHARGY ( 7 FDA reports)
LEUKOCYTURIA ( 7 FDA reports)
LIPASE INCREASED ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
LUNG CONSOLIDATION ( 7 FDA reports)
MONONUCLEOSIS SYNDROME ( 7 FDA reports)
MUSCLE RIGIDITY ( 7 FDA reports)
NEUROPATHY PERIPHERAL ( 7 FDA reports)
NEUROTOXICITY ( 7 FDA reports)
NYSTAGMUS ( 7 FDA reports)
PHOTOSENSITIVITY REACTION ( 7 FDA reports)
PNEUMONITIS ( 7 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 7 FDA reports)
SKIN ULCER ( 7 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 7 FDA reports)
THERAPY NON-RESPONDER ( 7 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 7 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 7 FDA reports)
UNRESPONSIVE TO STIMULI ( 7 FDA reports)
VASCULITIS ( 7 FDA reports)
VENOOCCLUSIVE DISEASE ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ACUTE LEFT VENTRICULAR FAILURE ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 6 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 6 FDA reports)
ANAEMIA NEONATAL ( 6 FDA reports)
APHASIA ( 6 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 6 FDA reports)
ARTHRITIS ( 6 FDA reports)
ATROPHIC GLOSSITIS ( 6 FDA reports)
AZOTAEMIA ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BLOOD POTASSIUM DECREASED ( 6 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 6 FDA reports)
CYSTITIS HAEMORRHAGIC ( 6 FDA reports)
EMOTIONAL DISTRESS ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
ENCEPHALITIS ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
EPILEPSY ( 6 FDA reports)
FLATULENCE ( 6 FDA reports)
FOETAL ARRHYTHMIA ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GASTROENTERITIS ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
HEPATIC NECROSIS ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
HYPOPROTEINAEMIA ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
INTESTINAL ISCHAEMIA ( 6 FDA reports)
ISCHAEMIA ( 6 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 6 FDA reports)
LOBAR PNEUMONIA ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
MALNUTRITION ( 6 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 6 FDA reports)
MYCOBACTERIUM ABSCESSUS INFECTION ( 6 FDA reports)
MYOCARDITIS MYCOTIC ( 6 FDA reports)
NEUTROPENIC SEPSIS ( 6 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 6 FDA reports)
OPTIC NERVE DISORDER ( 6 FDA reports)
PANCREATITIS HAEMORRHAGIC ( 6 FDA reports)
PARACENTESIS ABDOMEN ( 6 FDA reports)
PRODUCT COLOUR ISSUE ( 6 FDA reports)
PRODUCT TASTE ABNORMAL ( 6 FDA reports)
RESPIRATORY DEPRESSION ( 6 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 6 FDA reports)
RESPIRATORY TRACT HAEMORRHAGE ( 6 FDA reports)
RESPIRATORY TRACT INFECTION ( 6 FDA reports)
SCEDOSPORIUM INFECTION ( 6 FDA reports)
SKIN REACTION ( 6 FDA reports)
TOXIC ENCEPHALOPATHY ( 6 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 6 FDA reports)
WOUND INFECTION ( 6 FDA reports)
WOUND TREATMENT ( 6 FDA reports)
ZYGOMYCOSIS ( 6 FDA reports)
ABDOMINAL ABSCESS ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 5 FDA reports)
APPLICATION SITE REACTION ( 5 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
BOVINE TUBERCULOSIS ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CEREBRAL ATROPHY ( 5 FDA reports)
CEREBRAL INFARCTION ( 5 FDA reports)
CHOLANGITIS ACUTE ( 5 FDA reports)
COAGULATION FACTOR DECREASED ( 5 FDA reports)
CULTURE POSITIVE ( 5 FDA reports)
CULTURE STOOL POSITIVE ( 5 FDA reports)
DEAFNESS BILATERAL ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
ENTEROBACTER INFECTION ( 5 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 5 FDA reports)
ESCHERICHIA SEPSIS ( 5 FDA reports)
EYE PAIN ( 5 FDA reports)
EYELID OEDEMA ( 5 FDA reports)
FLUSHING ( 5 FDA reports)
FOETAL GROWTH RETARDATION ( 5 FDA reports)
GASTROINTESTINAL TOXICITY ( 5 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HEPATOCELLULAR DAMAGE ( 5 FDA reports)
HIV INFECTION ( 5 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 5 FDA reports)
HYPOTHERMIA ( 5 FDA reports)
HYPOTONIA ( 5 FDA reports)
IATROGENIC INJURY ( 5 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL DECREASED ( 5 FDA reports)
INTESTINAL INFARCTION ( 5 FDA reports)
LIVEDO RETICULARIS ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 5 FDA reports)
LUNG INFILTRATION ( 5 FDA reports)
LYMPHOPENIA ( 5 FDA reports)
MITRAL VALVE INCOMPETENCE ( 5 FDA reports)
NEONATAL HYPOXIA ( 5 FDA reports)
NEPHRITIS INTERSTITIAL ( 5 FDA reports)
OPEN WOUND ( 5 FDA reports)
ORAL CANDIDIASIS ( 5 FDA reports)
ORGAN FAILURE ( 5 FDA reports)
PANCREATITIS CHRONIC ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 5 FDA reports)
PRODUCTIVE COUGH ( 5 FDA reports)
PROTEIN TOTAL DECREASED ( 5 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 5 FDA reports)
PULMONARY CONGESTION ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
PULMONARY FIBROSIS ( 5 FDA reports)
PULMONARY TUBERCULOSIS ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RASH VESICULAR ( 5 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 5 FDA reports)
SCAR ( 5 FDA reports)
SKIN TEST POSITIVE ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
STREPTOCOCCAL INFECTION ( 5 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 5 FDA reports)
SUBDURAL HAEMATOMA ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
SYSTEMIC CANDIDA ( 5 FDA reports)
THROMBOCYTOPENIA NEONATAL ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
TRAUMATIC BRAIN INJURY ( 5 FDA reports)
UROSEPSIS ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
ACID FAST BACILLI INFECTION ( 4 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 4 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 4 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
AORTIC ANEURYSM ( 4 FDA reports)
BACTERIAL TOXAEMIA ( 4 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 4 FDA reports)
BLOOD CALCIUM DECREASED ( 4 FDA reports)
CACHEXIA ( 4 FDA reports)
CANCER PAIN ( 4 FDA reports)
CARDIAC TAMPONADE ( 4 FDA reports)
CATHETER RELATED INFECTION ( 4 FDA reports)
CELLULITIS GANGRENOUS ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
CHOKING SENSATION ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
COLLAGEN DISORDER ( 4 FDA reports)
DECUBITUS ULCER ( 4 FDA reports)
DERMATITIS ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
ELECTROCARDIOGRAM REPOLARISATION ABNORMALITY ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ENCEPHALITIS FUNGAL ( 4 FDA reports)
EPIDERMAL NECROSIS ( 4 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FIBRIN D DIMER INCREASED ( 4 FDA reports)
FISTULA ( 4 FDA reports)
FOETAL GROWTH RESTRICTION ( 4 FDA reports)
FUNGAL PERITONITIS ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROINTESTINAL FISTULA ( 4 FDA reports)
GRAFT THROMBOSIS ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATITIS ACUTE ( 4 FDA reports)
HEPATITIS B ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HODGKIN'S DISEASE ( 4 FDA reports)
HYPERREFLEXIA ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
INFANTILE APNOEIC ATTACK ( 4 FDA reports)
INFUSION SITE REACTION ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
KLEBSIELLA SEPSIS ( 4 FDA reports)
LEUKAEMIA ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LUNG NEOPLASM ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
LYMPHOCYTIC INFILTRATION ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MENINGITIS ( 4 FDA reports)
METABOLIC ENCEPHALOPATHY ( 4 FDA reports)
MIDDLE EAR EFFUSION ( 4 FDA reports)
MIOSIS ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
MYOPERICARDITIS ( 4 FDA reports)
NEUROLOGICAL SYMPTOM ( 4 FDA reports)
NEUROSIS ( 4 FDA reports)
NEUTROPENIC INFECTION ( 4 FDA reports)
NEUTROPHIL COUNT INCREASED ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PAPULE ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PERIPHERAL EMBOLISM ( 4 FDA reports)
PERIPHERAL ISCHAEMIA ( 4 FDA reports)
PERIVASCULAR DERMATITIS ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PNEUMONIA ASPIRATION ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 4 FDA reports)
PROTEUS INFECTION ( 4 FDA reports)
PSEUDOMONAL SEPSIS ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RENAL FAILURE NEONATAL ( 4 FDA reports)
RENAL INJURY ( 4 FDA reports)
RENAL ISCHAEMIA ( 4 FDA reports)
RENAL TUBULAR ACIDOSIS ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SERRATIA INFECTION ( 4 FDA reports)
SHOCK HAEMORRHAGIC ( 4 FDA reports)
SKIN INDURATION ( 4 FDA reports)
SKIN NECROSIS ( 4 FDA reports)
SWELLING ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
TORTICOLLIS ( 4 FDA reports)
TOXIC NEUROPATHY ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
ULCER ( 4 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
URTICARIA GENERALISED ( 4 FDA reports)
URTICARIA PAPULAR ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
AIDS RELATED COMPLICATION ( 3 FDA reports)
AORTIC VALVE INCOMPETENCE ( 3 FDA reports)
APATHY ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
APLASTIC ANAEMIA ( 3 FDA reports)
ARTERIAL RUPTURE ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 3 FDA reports)
AUTOANTIBODY POSITIVE ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD BICARBONATE DECREASED ( 3 FDA reports)
BLOOD DISORDER ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 3 FDA reports)
BLOOD PRESSURE ABNORMAL ( 3 FDA reports)
BONE MARROW DISORDER ( 3 FDA reports)
BONE MARROW TRANSPLANT ( 3 FDA reports)
BRADYCARDIA NEONATAL ( 3 FDA reports)
BRAIN ABSCESS ( 3 FDA reports)
BRAIN DAMAGE ( 3 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 3 FDA reports)
BREATH SOUNDS ABNORMAL ( 3 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 3 FDA reports)
CALCIPHYLAXIS ( 3 FDA reports)
CARDIAC FAILURE ACUTE ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CAUDA EQUINA SYNDROME ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 3 FDA reports)
CITROBACTER INFECTION ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COMA SCALE ABNORMAL ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
CONJUNCTIVITIS ( 3 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 3 FDA reports)
CORYNEBACTERIUM INFECTION ( 3 FDA reports)
CREPITATIONS ( 3 FDA reports)
CSF TEST ABNORMAL ( 3 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DRUG ADMINISTRATION ERROR ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
ENGRAFT FAILURE ( 3 FDA reports)
ENTERITIS ( 3 FDA reports)
EPIGASTRIC DISCOMFORT ( 3 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 3 FDA reports)
EXTREMITY CONTRACTURE ( 3 FDA reports)
EYE INFLAMMATION ( 3 FDA reports)
FEBRILE INFECTION ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FLANK PAIN ( 3 FDA reports)
FOETAL HEART RATE DISORDER ( 3 FDA reports)
GASTRIC PERFORATION ( 3 FDA reports)
GASTROINTESTINAL HYPOMOTILITY ( 3 FDA reports)
GLOMERULONEPHRITIS ( 3 FDA reports)
GRAFT COMPLICATION ( 3 FDA reports)
HAEMATOCHEZIA ( 3 FDA reports)
HAEMATOTOXICITY ( 3 FDA reports)
HAEMOLYSIS ( 3 FDA reports)
HAEMORRHAGE URINARY TRACT ( 3 FDA reports)
HAND AMPUTATION ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEART SOUNDS ABNORMAL ( 3 FDA reports)
HEPATIC FIBROSIS ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HUMAN HERPESVIRUS 6 INFECTION ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
HYPERCALCAEMIA ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPEROXALURIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
ILEAL PERFORATION ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
IMMEDIATE POST-INJECTION REACTION ( 3 FDA reports)
IMMUNE SYSTEM DISORDER ( 3 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 3 FDA reports)
IMPAIRED HEALING ( 3 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
JOINT CONTRACTURE ( 3 FDA reports)
LIP DISORDER ( 3 FDA reports)
MACULAR OEDEMA ( 3 FDA reports)
MARROW HYPERPLASIA ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MENINGITIS TUBERCULOUS ( 3 FDA reports)
MESENTERIC ARTERY THROMBOSIS ( 3 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 3 FDA reports)
MUTISM ( 3 FDA reports)
MYELODYSPLASTIC SYNDROME ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
MYOSITIS ( 3 FDA reports)
NEPHROCALCINOSIS ( 3 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 3 FDA reports)
NEPHROPATHY ( 3 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 3 FDA reports)
NEUTROPENIC COLITIS ( 3 FDA reports)
NIKOLSKY'S SIGN ( 3 FDA reports)
OPTIC NEURITIS RETROBULBAR ( 3 FDA reports)
PARADOXICAL DRUG REACTION ( 3 FDA reports)
PARAKERATOSIS ( 3 FDA reports)
PARONYCHIA ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PLATELET COUNT INCREASED ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PNEUMONIA VIRAL ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PRURIGO ( 3 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 3 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULSE ABSENT ( 3 FDA reports)
PULSE PRESSURE DECREASED ( 3 FDA reports)
PURULENCE ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
QUADRIPARESIS ( 3 FDA reports)
RED MAN SYNDROME ( 3 FDA reports)
RENAL CYST ( 3 FDA reports)
RESPIRATORY ACIDOSIS ( 3 FDA reports)
RESPIRATORY TRACT CONGESTION ( 3 FDA reports)
RIGHT VENTRICULAR FAILURE ( 3 FDA reports)
SALMONELLA SEPSIS ( 3 FDA reports)
SCLEREMA ( 3 FDA reports)
SEPSIS SYNDROME ( 3 FDA reports)
SERUM SICKNESS-LIKE REACTION ( 3 FDA reports)
SHORT-BOWEL SYNDROME ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN FIBROSIS ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SPLEEN DISORDER ( 3 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 3 FDA reports)
STEM CELL TRANSPLANT ( 3 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 3 FDA reports)
STRESS ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUPERINFECTION ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TONGUE DISORDER ( 3 FDA reports)
TRACHEAL HAEMORRHAGE ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
VACCINATION FAILURE ( 3 FDA reports)
VAGINAL CELLULITIS ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
VASCULAR PSEUDOANEURYSM ( 3 FDA reports)
VASCULITIS CEREBRAL ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABORTION ( 2 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 2 FDA reports)
ACUTE MEGAKARYOCYTIC LEUKAEMIA ( 2 FDA reports)
ACUTE PRERENAL FAILURE ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALANINE AMINOTRANSFERASE ABNORMAL ( 2 FDA reports)
AMAUROSIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
ANASTOMOTIC HAEMORRHAGE ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANTIBIOTIC LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
APHTHOUS STOMATITIS ( 2 FDA reports)
APNOEA ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
APPLICATION SITE CELLULITIS ( 2 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
ARTHRITIS INFECTIVE ( 2 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 2 FDA reports)
ATRIAL SEPTAL DEFECT ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BACTEROIDES INFECTION ( 2 FDA reports)
BENIGN INTRACRANIAL HYPERTENSION ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BILIARY CIRRHOSIS ( 2 FDA reports)
BLAST CRISIS IN MYELOGENOUS LEUKAEMIA ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE DECREASED ( 2 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 2 FDA reports)
BLOOD CHLORIDE INCREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD SODIUM INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD UREA DECREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BODY TEMPERATURE DECREASED ( 2 FDA reports)
BONE MARROW NECROSIS ( 2 FDA reports)
BONE MARROW TOXICITY ( 2 FDA reports)
BRADYPNOEA ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST NEONATAL ( 2 FDA reports)
CATHETER BACTERAEMIA ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 2 FDA reports)
CEREBELLAR SYNDROME ( 2 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHROMATOPSIA ( 2 FDA reports)
CHRONIC SINUSITIS ( 2 FDA reports)
CLONUS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CNS VENTRICULITIS ( 2 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLON ADENOMA ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONGENITAL MALARIA ( 2 FDA reports)
CONGENITAL TRICUSPID VALVE ATRESIA ( 2 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 2 FDA reports)
CSF BACTERIA IDENTIFIED ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
CYST ( 2 FDA reports)
CYTOTOXIC OEDEMA ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DIASTOLIC DYSFUNCTION ( 2 FDA reports)
DILATATION ATRIAL ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISCOMFORT ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 2 FDA reports)
ECHOLALIA ( 2 FDA reports)
ECTHYMA ( 2 FDA reports)
ECZEMA ASTEATOTIC ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE DECREASED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENCEPHALITIC INFECTION ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENDOPHTHALMITIS ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENGRAFTMENT SYNDROME ( 2 FDA reports)
ENTEROBACTER BACTERAEMIA ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
ENTEROCOCCUS TEST POSITIVE ( 2 FDA reports)
ENTEROCOLITIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 2 FDA reports)
ESCHERICHIA TEST POSITIVE ( 2 FDA reports)
EXFOLIATIVE RASH ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
EXTRAVASATION ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EXTUBATION ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEEDING DISORDER NEONATAL ( 2 FDA reports)
FEEDING TUBE COMPLICATION ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FINGER AMPUTATION ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTROENTERITIS CLOSTRIDIAL ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GENE MUTATION IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GINGIVAL DISORDER ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GOUT ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
GRANULOCYTE COUNT INCREASED ( 2 FDA reports)
H1N1 INFLUENZA ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HEART DISEASE CONGENITAL ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC HAEMORRHAGE ( 2 FDA reports)
HEPATIC ISCHAEMIA ( 2 FDA reports)
HEPATOSPLENOMEGALY NEONATAL ( 2 FDA reports)
HERPES SIMPLEX SEROLOGY POSITIVE ( 2 FDA reports)
HUMAN HERPES VIRUS 8 TEST POSITIVE ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 2 FDA reports)
HYPERVITAMINOSIS A ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOVITAMINOSIS ( 2 FDA reports)
ILEOSTOMY ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMMUNOSUPPRESSION ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION RATE ( 2 FDA reports)
INFECTIOUS PERITONITIS ( 2 FDA reports)
INFLUENZA A VIRUS TEST POSITIVE ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INJECTION SITE SWELLING ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
IRIDOCYCLITIS ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
KIDNEY FIBROSIS ( 2 FDA reports)
KLEBSIELLA TEST POSITIVE ( 2 FDA reports)
LARGE INTESTINAL ULCER ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LEUKAEMIA RECURRENT ( 2 FDA reports)
LEUKODYSTROPHY ( 2 FDA reports)
LIFE SUPPORT ( 2 FDA reports)
LINEAR IGA DISEASE ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVER ABSCESS ( 2 FDA reports)
LUNG HERNIA ( 2 FDA reports)
LUNG TRANSPLANT REJECTION ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE INCREASED ( 2 FDA reports)
LYMPHOCYTIC DERMATITIS ( 2 FDA reports)
LYMPHOCYTOSIS ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MALARIA ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENINGEAL DISORDER ( 2 FDA reports)
MENINGITIS BACTERIAL ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
METABOLIC FUNCTION TEST ABNORMAL ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MORGANELLA INFECTION ( 2 FDA reports)
MOTOR DYSFUNCTION ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYCOBACTERIUM CHELONAE INFECTION ( 2 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 2 FDA reports)
MYELOID MATURATION ARREST ( 2 FDA reports)
NECROTISING GRANULOMATOUS LYMPHADENITIS ( 2 FDA reports)
NEONATAL ASPIRATION ( 2 FDA reports)
NEONATAL HYPOTENSION ( 2 FDA reports)
NEONATAL INFECTION ( 2 FDA reports)
NEUROMUSCULAR BLOCK PROLONGED ( 2 FDA reports)
NEUROMUSCULAR BLOCKADE ( 2 FDA reports)
NEUROMYOPATHY ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NORMAL NEWBORN ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCULAR ICTERUS ( 2 FDA reports)
OEDEMA NEONATAL ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYP COLORECTAL ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROCEDURAL PAIN ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PULMONARY ARTERY THROMBOSIS ( 2 FDA reports)
PULMONARY INTERSTITIAL EMPHYSEMA SYNDROME ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RASH MORBILLIFORM ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL TUBULAR ATROPHY ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
RETICULOCYTE COUNT DECREASED ( 2 FDA reports)
RETICULOCYTOPENIA ( 2 FDA reports)
RETINAL INFARCTION ( 2 FDA reports)
RETINOIC ACID SYNDROME ( 2 FDA reports)
SALMONELLOSIS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SEROMA ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN EROSION ( 2 FDA reports)
SKIN INFECTION ( 2 FDA reports)
SKIN NODULE ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SMALL INTESTINAL PERFORATION ( 2 FDA reports)
SNORING ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL HAEMATOMA ( 2 FDA reports)
SPLENIC LESION ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
T-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
THROMBOSIS MESENTERIC VESSEL ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TONGUE EXFOLIATION ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY TRACT INFECTION PSEUDOMONAL ( 2 FDA reports)
URINARY TRACT OBSTRUCTION ( 2 FDA reports)
UTERINE CONTRACTIONS DURING PREGNANCY ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VENA CAVA THROMBOSIS ( 2 FDA reports)
VENOUS HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR ARRHYTHMIA ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VESTIBULAR DISORDER ( 2 FDA reports)
VIRAEMIA ( 2 FDA reports)
VISCERAL CONGESTION ( 2 FDA reports)
WHITE BLOOD CELL DISORDER ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
WOUND INFECTION FUNGAL ( 2 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
WRONG DRUG ADMINISTERED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ABDOMINAL NEOPLASM ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACINETOBACTER TEST POSITIVE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE ABDOMEN ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADENOVIRUS INFECTION ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
AMOEBIASIS ( 1 FDA reports)
AMYOTROPHY ( 1 FDA reports)
ANAL CANCER ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANASTOMOTIC COMPLICATION ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANTITHROMBIN III DECREASED ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE REPLACEMENT ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPLICATION SITE BURNING ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
ARACHNOIDITIS ( 1 FDA reports)
AREFLEXIA ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPERGILLUS TEST ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACILLUS TEST POSITIVE ( 1 FDA reports)
BACTERIA BLOOD IDENTIFIED ( 1 FDA reports)
BACTERIAL ANTIGEN POSITIVE ( 1 FDA reports)
BETA 2 MICROGLOBULIN URINE INCREASED ( 1 FDA reports)
BETA-N-ACETYL-D-GLUCOSAMINIDASE INCREASED ( 1 FDA reports)
BICUSPID AORTIC VALVE ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BILE OUTPUT ABNORMAL ( 1 FDA reports)
BILIARY DILATATION ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 1 FDA reports)
BLOOD AMYLASE DECREASED ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD CATECHOLAMINES INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD GALACTOSE INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD STEM CELL TRANSPLANT FAILURE ( 1 FDA reports)
BLOOD URIC ACID DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOODY AIRWAY DISCHARGE ( 1 FDA reports)
BONE DEBRIDEMENT ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN CONTUSION ( 1 FDA reports)
BRAIN STEM HAEMORRHAGE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST PROSTHESIS USER ( 1 FDA reports)
BREECH PRESENTATION ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHIECTASIS ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
BRONCHOPNEUMOPATHY ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
BURKITT'S LYMPHOMA ( 1 FDA reports)
BURNS SECOND DEGREE ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
C-REACTIVE PROTEIN DECREASED ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CANDIDA TEST POSITIVE ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC ENZYMES INCREASED ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC PACEMAKER REVISION ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIORENAL SYNDROME ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CD4 LYMPHOCYTES DECREASED ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL CALCIFICATION ( 1 FDA reports)
CEREBRAL CYST ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEMOTHERAPEUTIC DRUG LEVEL INCREASED ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHORIOAMNIONITIS ( 1 FDA reports)
CHORIORETINAL ATROPHY ( 1 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON GANGRENE ( 1 FDA reports)
COLON NEOPLASM ( 1 FDA reports)
COLONIC FISTULA ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLICATIONS OF BONE MARROW TRANSPLANT ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CONVULSION NEONATAL ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
COXSACKIE MYOCARDITIS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYSTAL NEPHROPATHY ( 1 FDA reports)
CSF CULTURE POSITIVE ( 1 FDA reports)
CULTURE WOUND POSITIVE ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
CYTOMEGALOVIRUS COLITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS OESOPHAGITIS ( 1 FDA reports)
CYTOMEGALOVIRUS TEST ( 1 FDA reports)
DEBRIDEMENT ( 1 FDA reports)
DECEREBRATION ( 1 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETIC FOOT ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG EFFECT PROLONGED ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRUG THERAPY CHANGED ( 1 FDA reports)
DRY GANGRENE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENANTHEMA ( 1 FDA reports)
ENDOCARDITIS BACTERIAL ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOMETRIAL HYPERPLASIA ( 1 FDA reports)
ENDOTOXIC SHOCK ( 1 FDA reports)
ENTERITIS NECROTICANS ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
ENTEROBACTER SEPSIS ( 1 FDA reports)
ENTEROBACTER TEST POSITIVE ( 1 FDA reports)
ENTEROCUTANEOUS FISTULA ( 1 FDA reports)
ENTEROVIRUS INFECTION ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE INFECTION FUNGAL ( 1 FDA reports)
EYE INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
FANCONI SYNDROME ACQUIRED ( 1 FDA reports)
FEBRILE CONVULSION ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FUNGAL ENDOCARDITIS ( 1 FDA reports)
FUNGAL TEST POSITIVE ( 1 FDA reports)
FUSARIUM INFECTION ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROENTERITIS ADENOVIRUS ( 1 FDA reports)
GASTROENTERITIS PSEUDOMONAS ( 1 FDA reports)
GASTROINTESTINAL CANDIDIASIS ( 1 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 1 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 1 FDA reports)
GLOMERULONEPHRITIS ACUTE ( 1 FDA reports)
GLYCOGEN STORAGE DISEASE TYPE II ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GRAVITATIONAL OEDEMA ( 1 FDA reports)
HAEMANGIOMA OF LIVER ( 1 FDA reports)
HAEMATOLOGY TEST ABNORMAL ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC CANDIDIASIS ( 1 FDA reports)
HEPATIC LESION ( 1 FDA reports)
HEPATIC SIDEROSIS ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HERNIAL EVENTRATION ( 1 FDA reports)
HERPES OPHTHALMIC ( 1 FDA reports)
HERPES ZOSTER OPHTHALMIC ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERADRENALISM ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERTENSION NEONATAL ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPERVIGILANCE ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOGLOBULINAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
IIIRD NERVE PARALYSIS ( 1 FDA reports)
ILEECTOMY ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMMUNOLOGY TEST ABNORMAL ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INCISION SITE COMPLICATION ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION PARASITIC ( 1 FDA reports)
INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS ( 1 FDA reports)
INFERTILITY ( 1 FDA reports)
INFLAMMATORY BOWEL DISEASE ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INTESTINAL HAEMORRHAGE ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
INTUBATION COMPLICATION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRON OVERLOAD ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JUGULAR VEIN THROMBOSIS ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACTOBACILLUS INFECTION ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LATE METABOLIC ACIDOSIS OF NEWBORN ( 1 FDA reports)
LEUKAEMIC INFILTRATION HEPATIC ( 1 FDA reports)
LEUKOPENIA NEONATAL ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER GRAFT LOSS ( 1 FDA reports)
LIVER TRANSPLANT REJECTION ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCKED-IN SYNDROME ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPH NODE PALPABLE ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
LYMPHOEDEMA ( 1 FDA reports)
MACROCEPHALY ( 1 FDA reports)
MACULAR ISCHAEMIA ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MARASMUS ( 1 FDA reports)
MASS ( 1 FDA reports)
MASTITIS BACTERIAL ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MEDIASTINITIS ( 1 FDA reports)
MEDICATION TAMPERING ( 1 FDA reports)
MENINGISM ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MESENTERIC OCCLUSION ( 1 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOANING ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOUTH BREATHING ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE INJURY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYOCARDIAL FIBROSIS ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
MYOPIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEONATAL ANURIA ( 1 FDA reports)
NEONATAL ASPHYXIA ( 1 FDA reports)
NEONATAL CARDIAC FAILURE ( 1 FDA reports)
NEONATAL HYPONATRAEMIA ( 1 FDA reports)
NEONATAL PNEUMONIA ( 1 FDA reports)
NEONATAL RESPIRATORY ACIDOSIS ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROGENIC SHOCK ( 1 FDA reports)
NEUROLOGICAL EXAMINATION ABNORMAL ( 1 FDA reports)
NEUTROPENIA NEONATAL ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NOCARDIOSIS ( 1 FDA reports)
NODDING OF HEAD ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING ABNORMAL ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULAR HYPERTENSION ( 1 FDA reports)
OEDEMATOUS PANCREATITIS ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL INFECTION ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
ONYCHOMADESIS ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
OPTIC NERVE INFARCTION ( 1 FDA reports)
OPTIC NERVE INJURY ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORAL SOFT TISSUE DISORDER ( 1 FDA reports)
ORGAN TRANSPLANT ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OXYGEN SUPPLEMENTATION ( 1 FDA reports)
PALPABLE PURPURA ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PANCREATIC ENZYMES INCREASED ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PARVOVIRUS B19 TEST POSITIVE ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONEAL HAEMORRHAGE ( 1 FDA reports)
PERITONEAL NECROSIS ( 1 FDA reports)
PERSEVERATION ( 1 FDA reports)
PHARYNGEAL NEOPLASM ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHYSICAL EXAMINATION ABNORMAL ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLASMACYTOMA ( 1 FDA reports)
PLEURAL INFECTION ( 1 FDA reports)
PNEUMONECTOMY ( 1 FDA reports)
PNEUMONIA NECROTISING ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PORENCEPHALY ( 1 FDA reports)
PORTAL VEIN THROMBOSIS ( 1 FDA reports)
POST PROCEDURAL BILE LEAK ( 1 FDA reports)
POSTMATURE BABY ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PREMATURE RUPTURE OF MEMBRANES ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATIC ADENOMA ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEUS TEST POSITIVE ( 1 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 1 FDA reports)
PSOAS ABSCESS ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY RENAL SYNDROME ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY VASCULAR DISORDER ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUNCTATE KERATITIS ( 1 FDA reports)
PUNCTURE SITE REACTION ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH SCARLATINIFORM ( 1 FDA reports)
RECTAL ABSCESS ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL HAEMORRHAGE ( 1 FDA reports)
RENAL NECROSIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION VIRAL ( 1 FDA reports)
RETINAL DEGENERATION ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETINAL VASCULITIS ( 1 FDA reports)
RETROPERITONEAL LYMPHADENOPATHY ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
SALIVARY HYPERSECRETION ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SERRATIA SEPSIS ( 1 FDA reports)
SIDEROBLASTIC ANAEMIA ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SKIN DESQUAMATION ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPINAL OSTEOARTHRITIS ( 1 FDA reports)
SPINAL SHOCK ( 1 FDA reports)
SPLENIC HAEMATOMA ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STEROID WITHDRAWAL SYNDROME ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS NECROTISING ( 1 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
SYMBLEPHARON ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYSTOLIC DYSFUNCTION ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBIN-ANTITHROMBIN III COMPLEX INCREASED ( 1 FDA reports)
THROMBOPHLEBITIS SEPTIC ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TONIC CLONIC MOVEMENTS ( 1 FDA reports)
TONSILLAR ULCER ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC SHOCK SYNDROME STREPTOCOCCAL ( 1 FDA reports)
TOXICOLOGIC TEST ABNORMAL ( 1 FDA reports)
TRACHEOBRONCHITIS ( 1 FDA reports)
TRANSFUSION-TRANSMITTED INFECTIOUS DISEASE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUBERCULIN TEST POSITIVE ( 1 FDA reports)
TUMOUR FLARE ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
TYPE 2 LEPRA REACTION ( 1 FDA reports)
TYPHOID FEVER ( 1 FDA reports)
ULCERATIVE KERATITIS ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
ULTRASOUND SKULL ABNORMAL ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION STAPHYLOCOCCAL ( 1 FDA reports)
URINARY TRACT INFECTION VIRAL ( 1 FDA reports)
URTICARIA PIGMENTOSA ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASOGENIC CEREBRAL OEDEMA ( 1 FDA reports)
VASOPLEGIA SYNDROME ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VENTRICULAR DYSKINESIA ( 1 FDA reports)
VENTRICULAR TACHYARRHYTHMIA ( 1 FDA reports)
VESSEL PUNCTURE SITE REACTION ( 1 FDA reports)
VIRUS URINE TEST POSITIVE ( 1 FDA reports)
VISCERAL LEISHMANIASIS ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT GAIN POOR ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND DECOMPOSITION ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use