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

PYREXIA ( 85 FDA reports)
RENAL FAILURE ACUTE ( 74 FDA reports)
CYTOLYTIC HEPATITIS ( 63 FDA reports)
ANAEMIA ( 62 FDA reports)
CONFUSIONAL STATE ( 54 FDA reports)
CHOLESTASIS ( 53 FDA reports)
THROMBOCYTOPENIA ( 53 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 39 FDA reports)
RENAL FAILURE ( 39 FDA reports)
DRUG INTERACTION ( 38 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 37 FDA reports)
HAEMATURIA ( 37 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 35 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 34 FDA reports)
VOMITING ( 34 FDA reports)
NEUTROPENIA ( 33 FDA reports)
LEUKOPENIA ( 32 FDA reports)
PAIN ( 32 FDA reports)
LUNG DISORDER ( 31 FDA reports)
STEVENS-JOHNSON SYNDROME ( 31 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 30 FDA reports)
NAUSEA ( 30 FDA reports)
RASH MACULO-PAPULAR ( 30 FDA reports)
HYPOTENSION ( 29 FDA reports)
PLEURAL EFFUSION ( 29 FDA reports)
AGITATION ( 28 FDA reports)
CONDITION AGGRAVATED ( 28 FDA reports)
PRURITUS ( 28 FDA reports)
DYSPNOEA ( 27 FDA reports)
OLIGURIA ( 27 FDA reports)
RASH ( 27 FDA reports)
SEPTIC SHOCK ( 27 FDA reports)
DRUG INEFFECTIVE ( 26 FDA reports)
ERYTHEMA ( 26 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 25 FDA reports)
HYPONATRAEMIA ( 25 FDA reports)
MALAISE ( 25 FDA reports)
TOXIC SKIN ERUPTION ( 25 FDA reports)
PANCREATITIS ACUTE ( 24 FDA reports)
RESPIRATORY DISTRESS ( 24 FDA reports)
SEPSIS ( 24 FDA reports)
ANAPHYLACTIC SHOCK ( 23 FDA reports)
LYMPHOPENIA ( 22 FDA reports)
PANCYTOPENIA ( 22 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 20 FDA reports)
AGRANULOCYTOSIS ( 20 FDA reports)
INFLAMMATION ( 20 FDA reports)
FALL ( 19 FDA reports)
LYMPHADENOPATHY ( 19 FDA reports)
OEDEMA PERIPHERAL ( 19 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 19 FDA reports)
ANURIA ( 18 FDA reports)
HEADACHE ( 18 FDA reports)
INTERSTITIAL LUNG DISEASE ( 18 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 17 FDA reports)
CARDIAC ARREST ( 17 FDA reports)
COMA ( 17 FDA reports)
EOSINOPHILIA ( 17 FDA reports)
HEPATITIS CHOLESTATIC ( 17 FDA reports)
HYPOXIA ( 17 FDA reports)
PNEUMONIA ( 17 FDA reports)
SOMNOLENCE ( 17 FDA reports)
URTICARIA ( 17 FDA reports)
FACE OEDEMA ( 16 FDA reports)
HALLUCINATION, VISUAL ( 16 FDA reports)
HYPERTENSION ( 16 FDA reports)
ACUTE PULMONARY OEDEMA ( 15 FDA reports)
FATIGUE ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
ABDOMINAL PAIN ( 14 FDA reports)
BRADYCARDIA ( 14 FDA reports)
CIRCULATORY COLLAPSE ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
DERMATITIS BULLOUS ( 14 FDA reports)
ENCEPHALOPATHY ( 14 FDA reports)
GENERALISED ERYTHEMA ( 14 FDA reports)
HAEMOGLOBIN DECREASED ( 14 FDA reports)
PREMATURE BABY ( 14 FDA reports)
ASTHENIA ( 13 FDA reports)
CARDIO-RESPIRATORY ARREST ( 13 FDA reports)
DEEP VEIN THROMBOSIS ( 13 FDA reports)
DIARRHOEA ( 13 FDA reports)
HEPATITIS ( 13 FDA reports)
PULMONARY EMBOLISM ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
DISORIENTATION ( 12 FDA reports)
HALLUCINATION ( 12 FDA reports)
LIVER INJURY ( 12 FDA reports)
OXYGEN SATURATION DECREASED ( 12 FDA reports)
RASH PUSTULAR ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
DISEASE PROGRESSION ( 11 FDA reports)
HAEMATOMA ( 11 FDA reports)
LEUKOCYTOSIS ( 11 FDA reports)
LIVER DISORDER ( 11 FDA reports)
MULTI-ORGAN FAILURE ( 11 FDA reports)
PERIVENTRICULAR LEUKOMALACIA ( 11 FDA reports)
SHOCK HAEMORRHAGIC ( 11 FDA reports)
STAPHYLOCOCCAL INFECTION ( 11 FDA reports)
BACTERIAL SEPSIS ( 10 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
BONE MARROW FAILURE ( 10 FDA reports)
DELIRIUM ( 10 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 10 FDA reports)
HEPATOCELLULAR INJURY ( 10 FDA reports)
HYPERHIDROSIS ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
PARAESTHESIA ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
APLASIA ( 9 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
CHOLELITHIASIS ( 9 FDA reports)
DENTAL CARIES ( 9 FDA reports)
GINGIVAL DISORDER ( 9 FDA reports)
HEPATIC ENZYME INCREASED ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 9 FDA reports)
LYMPHOCYTOSIS ( 9 FDA reports)
MONOPLEGIA ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
OEDEMA ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
PERIPHERAL NERVE LESION ( 9 FDA reports)
POOR PERSONAL HYGIENE ( 9 FDA reports)
PRODUCT QUALITY ISSUE ( 9 FDA reports)
RESPIRATORY FAILURE ( 9 FDA reports)
SALIVA ALTERED ( 9 FDA reports)
STATUS EPILEPTICUS ( 9 FDA reports)
TOOTH LOSS ( 9 FDA reports)
ANGIOEDEMA ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
BRONCHOSPASM ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
EYELID OEDEMA ( 8 FDA reports)
HAEMOLYTIC ANAEMIA ( 8 FDA reports)
LIPASE INCREASED ( 8 FDA reports)
MONOCYTOSIS ( 8 FDA reports)
MUSCULAR WEAKNESS ( 8 FDA reports)
PAIN IN EXTREMITY ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
TORSADE DE POINTES ( 8 FDA reports)
VITAMIN D DEFICIENCY ( 8 FDA reports)
ARTHRALGIA ( 7 FDA reports)
ASPIRATION ( 7 FDA reports)
BLOOD BILIRUBIN INCREASED ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
FOETAL GROWTH RETARDATION ( 7 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 7 FDA reports)
HEPATITIS ACUTE ( 7 FDA reports)
HEPATOCELLULAR DAMAGE ( 7 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 7 FDA reports)
HUMAN HERPESVIRUS 8 INFECTION ( 7 FDA reports)
HYPOPHOSPHATAEMIA ( 7 FDA reports)
JAUNDICE NEONATAL ( 7 FDA reports)
KAPOSI'S SARCOMA ( 7 FDA reports)
LEUKOENCEPHALOPATHY ( 7 FDA reports)
LOGORRHOEA ( 7 FDA reports)
NECROTISING FASCIITIS ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
PURPURA ( 7 FDA reports)
RALES ( 7 FDA reports)
RASH ERYTHEMATOUS ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
VENTRICULAR TACHYCARDIA ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 6 FDA reports)
ANOSOGNOSIA ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BLINDNESS TRANSIENT ( 6 FDA reports)
BONE ABSCESS ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
CHILLS ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
DEATH ( 6 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 6 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 6 FDA reports)
ENDODONTIC PROCEDURE ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
FLIGHT OF IDEAS ( 6 FDA reports)
FOETAL ARRHYTHMIA ( 6 FDA reports)
FOREIGN BODY ASPIRATION ( 6 FDA reports)
GASTROINTESTINAL ISCHAEMIA ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
HEPATOMEGALY ( 6 FDA reports)
HYPERBILIRUBINAEMIA ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
IRRITABILITY ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
OSTEONECROSIS ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
RHEUMATOID ARTHRITIS ( 6 FDA reports)
SUSPICIOUSNESS ( 6 FDA reports)
TREMOR ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ARTERIOSCLEROSIS ( 5 FDA reports)
ASCITES ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
CEREBRAL VENOUS THROMBOSIS ( 5 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 5 FDA reports)
CYST ( 5 FDA reports)
DENTAL NECROSIS ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
ENTEROBACTER INFECTION ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
FOETAL HEART RATE DISORDER ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HYPERTHERMIA ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
ILEITIS ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
JAW DISORDER ( 5 FDA reports)
LACTIC ACIDOSIS ( 5 FDA reports)
LUNG NEOPLASM ( 5 FDA reports)
MUSCLE HAEMORRHAGE ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NEONATAL RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
PALLOR ( 5 FDA reports)
PELVIC PAIN ( 5 FDA reports)
POST PROCEDURAL HAEMATOMA ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
RENAL TUBULAR DISORDER ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
SUBILEUS ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
TOOTH EXTRACTION ( 5 FDA reports)
TRANSAMINASES INCREASED ( 5 FDA reports)
ACCIDENTAL OVERDOSE ( 4 FDA reports)
AGGRESSION ( 4 FDA reports)
BLOOD PRESSURE DECREASED ( 4 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARDIOGENIC SHOCK ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DERMATITIS ALLERGIC ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
EPIDERMAL NECROSIS ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
ESCHERICHIA INFECTION ( 4 FDA reports)
FEMUR FRACTURE ( 4 FDA reports)
FOETAL GROWTH RESTRICTION ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
GINGIVITIS ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 4 FDA reports)
HERPES VIRUS INFECTION ( 4 FDA reports)
HYPERTHYROIDISM ( 4 FDA reports)
INFECTION ( 4 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 4 FDA reports)
LOOSE TOOTH ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MANIA ( 4 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
METASTASES TO BONE ( 4 FDA reports)
MONONUCLEOSIS SYNDROME ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
MYOCLONIC EPILEPSY ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
MYOSITIS ( 4 FDA reports)
NODAL RHYTHM ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PERIODONTITIS ( 4 FDA reports)
PETIT MAL EPILEPSY ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PNEUMOPERITONEUM ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RASH PAPULAR ( 4 FDA reports)
RENAL TUBULAR ACIDOSIS ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
SKIN DISORDER ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
VENTRICULAR HYPOKINESIA ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABDOMINAL WALL ABSCESS ( 3 FDA reports)
ABSCESS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE ABDOMEN ( 3 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
ANAEMIA NEONATAL ( 3 FDA reports)
ANAPHYLACTOID SHOCK ( 3 FDA reports)
ANOXIC ENCEPHALOPATHY ( 3 FDA reports)
APATHY ( 3 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ASPERGILLOSIS ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
BACTEROIDES INFECTION ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BLOOD LACTIC ACID INCREASED ( 3 FDA reports)
BLOOD OSMOLARITY DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BRAIN DEATH ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIOPULMONARY FAILURE ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
CONVERSION DISORDER ( 3 FDA reports)
CULTURE URINE POSITIVE ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 3 FDA reports)
DRUG ABUSER ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ERYSIPELAS ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGIC ANAEMIA ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOTHERMIA ( 3 FDA reports)
INJECTION SITE THROMBOSIS ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
MALLORY-WEISS SYNDROME ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MENINGEAL DISORDER ( 3 FDA reports)
MENINGITIS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PALATAL OEDEMA ( 3 FDA reports)
PANCREATIC NECROSIS ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PERIRENAL HAEMATOMA ( 3 FDA reports)
PLEURAL DISORDER ( 3 FDA reports)
PORTAL VEIN THROMBOSIS ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
SMALL INTESTINAL STENOSIS ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
T-CELL LYMPHOMA ( 3 FDA reports)
THROMBOPHLEBITIS ( 3 FDA reports)
TRANSPLANT REJECTION ( 3 FDA reports)
VANISHING BILE DUCT SYNDROME ( 3 FDA reports)
WALKING DISABILITY ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL SEPSIS ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ANAESTHETIC COMPLICATION ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
AV DISSOCIATION ( 2 FDA reports)
BACTERIA STOOL IDENTIFIED ( 2 FDA reports)
BACTERIAL TEST POSITIVE ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLEPHARITIS ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE ABNORMAL ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD URIC ACID DECREASED ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
CALCINOSIS ( 2 FDA reports)
CALCULUS URINARY ( 2 FDA reports)
CANDIDA SEPSIS ( 2 FDA reports)
CARBON DIOXIDE DECREASED ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CAUDA EQUINA SYNDROME ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CONTRAINDICATION TO MEDICAL TREATMENT ( 2 FDA reports)
CULTURE STOOL NEGATIVE ( 2 FDA reports)
DECREASED INSULIN REQUIREMENT ( 2 FDA reports)
DENERVATION ATROPHY ( 2 FDA reports)
DEPERSONALISATION ( 2 FDA reports)
DEPRESSIVE SYMPTOM ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG PRESCRIBING ERROR ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DUODENAL ULCER PERFORATION ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EPILEPSY ( 2 FDA reports)
ESCHERICHIA SEPSIS ( 2 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
FUNGAL SEPSIS ( 2 FDA reports)
GENITAL HERPES ( 2 FDA reports)
GENITAL ULCERATION ( 2 FDA reports)
GRANULOCYTES MATURATION ARREST ( 2 FDA reports)
GRANULOMA ( 2 FDA reports)
GROIN PAIN ( 2 FDA reports)
HAEMODYNAMIC INSTABILITY ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HYPERCHLORAEMIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 2 FDA reports)
IMPETIGO HERPETIFORMIS ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCISION SITE HAEMATOMA ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJECTION SITE REACTION ( 2 FDA reports)
INTESTINAL ISCHAEMIA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
JAUNDICE CHOLESTATIC ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LIVER TRANSPLANT REJECTION ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MENINGORRHAGIA ( 2 FDA reports)
MIXED HEPATOCELLULAR-CHOLESTATIC INJURY ( 2 FDA reports)
MORTON'S NEUROMA ( 2 FDA reports)
MOUTH ULCERATION ( 2 FDA reports)
MUCOSAL HAEMORRHAGE ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTIPLE INJURIES ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MYCOBACTERIA BLOOD TEST POSITIVE ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEOPLASM MALIGNANT ( 2 FDA reports)
NEOPLASM PROGRESSION ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVE COMPRESSION ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
OEDEMA GENITAL ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
PANNICULITIS ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PERITONEAL HAEMORRHAGE ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
PYELOCALIECTASIS ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
SCAR ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN PLAQUE ( 2 FDA reports)
SKIN TEST POSITIVE ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SPINAL FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TOBACCO ABUSE ( 2 FDA reports)
TOXIC ENCEPHALOPATHY ( 2 FDA reports)
TROPONIN INCREASED ( 2 FDA reports)
TRYPTASE INCREASED ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
TYPE I HYPERSENSITIVITY ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VASCULITIS NECROTISING ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE VESTIBULAR SYNDROME ( 1 FDA reports)
ADENOVIRAL HEPATITIS ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AMYLOIDOSIS ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANTIMITOCHONDRIAL ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ASPERGILLUS TEST POSITIVE ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN LUNG NEOPLASM ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY CIRRHOSIS ( 1 FDA reports)
BILIARY CYST ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS CORTICAL ( 1 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD CREATINE ABNORMAL ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD FOLATE DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
BONE MARROW MYELOGRAM ABNORMAL ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BONE MARROW TRANSPLANT ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRADYPNOEA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARBON DIOXIDE ABNORMAL ( 1 FDA reports)
CARDIAC AMYLOIDOSIS ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CATHETER SITE HAEMORRHAGE ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CD4/CD8 RATIO DECREASED ( 1 FDA reports)
CELL DEATH ( 1 FDA reports)
CELLULITIS STREPTOCOCCAL ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CHEMICAL POISONING ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLECYSTITIS INFECTIVE ( 1 FDA reports)
CHOLESTATIC LIVER INJURY ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
COAGULATION FACTOR DECREASED ( 1 FDA reports)
COAGULATION FACTOR VII LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR X LEVEL DECREASED ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER METASTATIC ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABDOMEN ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONNECTIVE TISSUE DISORDER ( 1 FDA reports)
CONSCIOUSNESS FLUCTUATING ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CRANIAL NEUROPATHY ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYSTALLURIA ( 1 FDA reports)
CSF WHITE BLOOD CELL COUNT POSITIVE ( 1 FDA reports)
CYST REMOVAL ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DEPENDENCE ON RESPIRATOR ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DERMO-HYPODERMITIS ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FAECAL VOMITING ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FANCONI SYNDROME ( 1 FDA reports)
FASCIITIS ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLUID IMBALANCE ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL AMYLOIDOSIS ( 1 FDA reports)
GASTROINTESTINAL TOXICITY ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVITIS ULCERATIVE ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTES ABNORMAL ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC ARTERY THROMBOSIS ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HEPATOBILIARY DISEASE ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HISTAMINE LEVEL INCREASED ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKALIURIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHERMIA MALIGNANT ( 1 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANT SITE WARMTH ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INTERCOSTAL RETRACTION ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRIDECTOMY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTURIA ( 1 FDA reports)
LIGHT CHAIN ANALYSIS INCREASED ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LISTERIOSIS ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOBLASTOSIS ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
MENINGORADICULITIS ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
MIOSIS ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MORGANELLA INFECTION ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUCKLE-WELLS SYNDROME ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME TRANSFORMATION ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEUROMYOPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NODAL ARRHYTHMIA ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OESOPHAGITIS ULCERATIVE ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANCREATOLITHIASIS ( 1 FDA reports)
PAPILLITIS ( 1 FDA reports)
PARAPARESIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PELIOSIS HEPATIS ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PH BODY FLUID ABNORMAL ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PITUITARY TUMOUR BENIGN ( 1 FDA reports)
PLATELET COUNT ABNORMAL ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAS BRONCHITIS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY RADIATION INJURY ( 1 FDA reports)
PULMONARY THROMBOSIS ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELONEPHRITIS ACUTE ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
PYRAMIDAL TRACT SYNDROME ( 1 FDA reports)
RADICULAR PAIN ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFRACTORY ANAEMIA ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL COLIC ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY ACIDOSIS ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF ESTEEM DECREASED ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SIMPLEX VIRUS TEST POSITIVE ( 1 FDA reports)
SKIN NECROSIS ( 1 FDA reports)
SKIN TEST NEGATIVE ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL INTESTINE OPERATION ( 1 FDA reports)
SPINAL CLAUDICATION ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SURGICAL FAILURE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENDON RUPTURE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRANSFUSION RELATED COMPLICATION ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
ULCER ( 1 FDA reports)
URINARY TRACT OBSTRUCTION ( 1 FDA reports)
URINE CALCIUM INCREASED ( 1 FDA reports)
URINE SODIUM INCREASED ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VITAMIN B12 DEFICIENCY ( 1 FDA reports)
WALKING AID USER ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
XEROSIS ( 1 FDA reports)

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