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

PYREXIA ( 96 FDA reports)
CONVULSION ( 72 FDA reports)
EPILEPSY ( 58 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 56 FDA reports)
RASH ( 54 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 51 FDA reports)
PLATELET COUNT DECREASED ( 51 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 50 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 46 FDA reports)
PNEUMONIA ( 44 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 39 FDA reports)
STATUS EPILEPTICUS ( 39 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 38 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 37 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 36 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 36 FDA reports)
SOMNOLENCE ( 35 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 35 FDA reports)
DRUG ERUPTION ( 31 FDA reports)
BLOOD CREATININE INCREASED ( 30 FDA reports)
LIVER DISORDER ( 30 FDA reports)
PNEUMONIA ASPIRATION ( 30 FDA reports)
ERYTHEMA ( 28 FDA reports)
RENAL FAILURE ACUTE ( 27 FDA reports)
GRAND MAL CONVULSION ( 26 FDA reports)
BLOOD UREA INCREASED ( 25 FDA reports)
INTERSTITIAL LUNG DISEASE ( 25 FDA reports)
RHABDOMYOLYSIS ( 25 FDA reports)
STEVENS-JOHNSON SYNDROME ( 25 FDA reports)
DIZZINESS ( 24 FDA reports)
DRUG INTERACTION ( 24 FDA reports)
FALL ( 24 FDA reports)
RASH PAPULAR ( 22 FDA reports)
AGRANULOCYTOSIS ( 21 FDA reports)
LOSS OF CONSCIOUSNESS ( 21 FDA reports)
ANAEMIA ( 20 FDA reports)
HAEMOGLOBIN DECREASED ( 20 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 19 FDA reports)
RENAL IMPAIRMENT ( 18 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 17 FDA reports)
NAUSEA ( 17 FDA reports)
BLOOD PRESSURE DECREASED ( 16 FDA reports)
DISEASE PROGRESSION ( 16 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 15 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 15 FDA reports)
CARDIAC FAILURE ( 15 FDA reports)
DRUG TOXICITY ( 15 FDA reports)
HYPONATRAEMIA ( 15 FDA reports)
SEPSIS ( 15 FDA reports)
CEREBRAL INFARCTION ( 14 FDA reports)
DYSLALIA ( 14 FDA reports)
HALLUCINATION ( 14 FDA reports)
INFECTION ( 14 FDA reports)
RESPIRATORY FAILURE ( 14 FDA reports)
SHOCK ( 14 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 13 FDA reports)
MALAISE ( 13 FDA reports)
OEDEMA PERIPHERAL ( 13 FDA reports)
VOMITING ( 13 FDA reports)
BLOOD SODIUM DECREASED ( 12 FDA reports)
DRUG HYPERSENSITIVITY ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
HAEMATOCRIT DECREASED ( 12 FDA reports)
HYPERKALAEMIA ( 12 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 12 FDA reports)
MULTI-ORGAN FAILURE ( 12 FDA reports)
PSYCHIATRIC SYMPTOM ( 12 FDA reports)
CHEST PAIN ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 11 FDA reports)
DRUG LEVEL INCREASED ( 11 FDA reports)
EOSINOPHIL COUNT INCREASED ( 11 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 11 FDA reports)
NEUTROPHIL COUNT DECREASED ( 11 FDA reports)
PARALYSIS ( 11 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
DERMATITIS EXFOLIATIVE ( 10 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 10 FDA reports)
RENAL DISORDER ( 10 FDA reports)
VENTRICULAR FIBRILLATION ( 10 FDA reports)
ASTHENIA ( 9 FDA reports)
BLOOD BILIRUBIN INCREASED ( 9 FDA reports)
BRAIN OEDEMA ( 9 FDA reports)
DISORIENTATION ( 9 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
GLIOBLASTOMA ( 9 FDA reports)
GRANULOCYTOPENIA ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
PULMONARY EMBOLISM ( 9 FDA reports)
RASH GENERALISED ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
TOXIC SKIN ERUPTION ( 9 FDA reports)
TREMOR ( 9 FDA reports)
BREECH PRESENTATION ( 8 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DELUSION ( 8 FDA reports)
DYSKINESIA ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
ERYTHEMA MULTIFORME ( 8 FDA reports)
FEBRILE NEUTROPENIA ( 8 FDA reports)
GESTATIONAL DIABETES ( 8 FDA reports)
GLIOBLASTOMA MULTIFORME ( 8 FDA reports)
HAEMODIALYSIS ( 8 FDA reports)
HALLUCINATION, VISUAL ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HEPATITIS FULMINANT ( 8 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 8 FDA reports)
HYPOAESTHESIA ( 8 FDA reports)
HYPOTENSION ( 8 FDA reports)
HYPOTHERMIA ( 8 FDA reports)
IRRITABILITY ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 8 FDA reports)
URINE OUTPUT DECREASED ( 8 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
BLOOD ALBUMIN DECREASED ( 7 FDA reports)
BLOOD POTASSIUM INCREASED ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 7 FDA reports)
HEMIPLEGIA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
HYPERTHERMIA ( 7 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 7 FDA reports)
ORAL MUCOSAL ERYTHEMA ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
VIRAL INFECTION ( 7 FDA reports)
AGGRESSION ( 6 FDA reports)
ALOPECIA ( 6 FDA reports)
ANEURYSM ( 6 FDA reports)
ANOREXIA ( 6 FDA reports)
BLOOD GLUCOSE INCREASED ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
BRAIN NEOPLASM ( 6 FDA reports)
CANDIDIASIS ( 6 FDA reports)
CEREBROVASCULAR OPERATION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DYSSTASIA ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GENERALISED ERYTHEMA ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 6 FDA reports)
PROTEIN TOTAL DECREASED ( 6 FDA reports)
RASH ERYTHEMATOUS ( 6 FDA reports)
SALIVARY HYPERSECRETION ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 5 FDA reports)
DEATH ( 5 FDA reports)
DIALYSIS ( 5 FDA reports)
DIARRHOEA ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HAEMATEMESIS ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
HYPOPHAGIA ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
METABOLIC ACIDOSIS ( 5 FDA reports)
NEOPLASM PROGRESSION ( 5 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 5 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
RASH PUSTULAR ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
RESPIRATORY DISORDER ( 5 FDA reports)
TONGUE ERUPTION ( 5 FDA reports)
TONGUE ULCERATION ( 5 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
APHONIA ( 4 FDA reports)
APLASIA PURE RED CELL ( 4 FDA reports)
ATROPHY ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BLOOD UREA DECREASED ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BONE MARROW DISORDER ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BRAIN HERNIATION ( 4 FDA reports)
BRUGADA SYNDROME ( 4 FDA reports)
CARDIAC FAILURE ACUTE ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
DENTAL OPERATION ( 4 FDA reports)
DERMATITIS ACNEIFORM ( 4 FDA reports)
DYSTONIA ( 4 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 4 FDA reports)
ENCEPHALITIS VIRAL ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EYE MOVEMENT DISORDER ( 4 FDA reports)
FOLLICULITIS ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 4 FDA reports)
GINGIVAL HYPERPLASIA ( 4 FDA reports)
HAND-FOOT-AND-MOUTH DISEASE ( 4 FDA reports)
HUMERUS FRACTURE ( 4 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
MENINGITIS BACTERIAL ( 4 FDA reports)
MUCOSAL EROSION ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
MYELODYSPLASTIC SYNDROME ( 4 FDA reports)
OSTEOMYELITIS ( 4 FDA reports)
PERNICIOUS ANAEMIA ( 4 FDA reports)
PNEUMONIA BACTERIAL ( 4 FDA reports)
PROTEIN URINE PRESENT ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RADIATION NECROSIS ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
URINARY INCONTINENCE ( 4 FDA reports)
UVEITIS ( 4 FDA reports)
VENTRICULAR TACHYCARDIA ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AKINESIA ( 3 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ATONIC SEIZURES ( 3 FDA reports)
BEDRIDDEN ( 3 FDA reports)
BICYTOPENIA ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BRADYARRHYTHMIA ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRAIN OPERATION ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CATHETER PLACEMENT ( 3 FDA reports)
CEREBRAL DECOMPRESSION ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DENTAL CARIES ( 3 FDA reports)
DENTAL PLAQUE ( 3 FDA reports)
DYSCHEZIA ( 3 FDA reports)
ENCEPHALITIS HERPES ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EVANS SYNDROME ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
GINGIVAL HYPERTROPHY ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HAEMORRHAGIC DIATHESIS ( 3 FDA reports)
HEPATIC CONGESTION ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATOCELLULAR DAMAGE ( 3 FDA reports)
HERPES VIRUS INFECTION ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
HYPERAEMIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERKINESIA ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
IMPETIGO ( 3 FDA reports)
INAPPROPRIATE AFFECT ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LEUKOENCEPHALOPATHY ( 3 FDA reports)
LIP OEDEMA ( 3 FDA reports)
LIPASE INCREASED ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MENINGITIS ASEPTIC ( 3 FDA reports)
MUCOUS MEMBRANE DISORDER ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 3 FDA reports)
ORAL MUCOSA EROSION ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
OXYGEN SUPPLEMENTATION ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PERFORMANCE STATUS DECREASED ( 3 FDA reports)
PERIODONTAL OPERATION ( 3 FDA reports)
PERIODONTITIS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 3 FDA reports)
PO2 DECREASED ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PURPURA ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
TOOTH DEPOSIT ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABNORMAL FAECES ( 2 FDA reports)
ABORTION INDUCED ( 2 FDA reports)
ABSCESS DRAINAGE ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANAEMIA MEGALOBLASTIC ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 2 FDA reports)
ANTICONVULSANT TOXICITY ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPARENT DEATH ( 2 FDA reports)
APPENDICITIS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BASOPHIL COUNT INCREASED ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD BRAIN BARRIER DEFECT ( 2 FDA reports)
BLOOD CALCIUM DECREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD CORTICOTROPHIN DECREASED ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD INSULIN INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
BRAIN ABSCESS ( 2 FDA reports)
BRAIN CONTUSION ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CEREBELLAR ATAXIA ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CLONIC CONVULSION ( 2 FDA reports)
COMA ( 2 FDA reports)
CONJUNCTIVAL DISCOLOURATION ( 2 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 2 FDA reports)
COUGH ( 2 FDA reports)
CRYING ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR INFECTION ( 2 FDA reports)
ELEVATED MOOD ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOETAL ANTICONVULSANT SYNDROME ( 2 FDA reports)
FOLATE DEFICIENCY ( 2 FDA reports)
GASTRIC POLYPS ( 2 FDA reports)
GASTROINTESTINAL HYPERMOTILITY ( 2 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 2 FDA reports)
GASTROINTESTINAL NEOPLASM ( 2 FDA reports)
GENITAL EROSION ( 2 FDA reports)
GENITAL RASH ( 2 FDA reports)
GINGIVAL OEDEMA ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEPATECTOMY ( 2 FDA reports)
HEPATIC ADENOMA ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HOMANS' SIGN ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HUMORAL IMMUNE DEFECT ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
HYPOTHALAMO-PITUITARY DISORDER ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILEUS PARALYTIC ( 2 FDA reports)
IMMUNODEFICIENCY ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
JOINT ANKYLOSIS ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIP EROSION ( 2 FDA reports)
LOGORRHOEA ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MANIA ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENINGITIS HAEMOPHILUS ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEOPLASM RECURRENCE ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OROPHARYNGEAL DISCOMFORT ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
OTORRHOEA ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA FUNGAL ( 2 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 2 FDA reports)
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RESPIRATORY MONILIASIS ( 2 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN HYPERPIGMENTATION ( 2 FDA reports)
STEREOTYPY ( 2 FDA reports)
STREPTOCOCCAL IDENTIFICATION TEST POSITIVE ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
STUPOR ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SUBDURAL HAEMORRHAGE ( 2 FDA reports)
SUBILEUS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THYROXINE DECREASED ( 2 FDA reports)
THYROXINE FREE DECREASED ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TONIC CONVULSION ( 2 FDA reports)
TOOTH AVULSION ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOOTH EROSION ( 2 FDA reports)
TOOTH INFECTION ( 2 FDA reports)
TOOTH RESORPTION ( 2 FDA reports)
TRI-IODOTHYRONINE DECREASED ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITAMIN B12 DECREASED ( 2 FDA reports)
ACCIDENT ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALBINISM ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BIOPSY LIVER ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD ELECTROLYTES ABNORMAL ( 1 FDA reports)
BLOOD PHOSPHORUS ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRAIN CANCER METASTATIC ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOREOATHETOSIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMA HEPATIC ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CONVULSIONS LOCAL ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
COPROPORPHYRINOGEN INCREASED ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EPENDYMOMA MALIGNANT ( 1 FDA reports)
ERYTHROPENIA ( 1 FDA reports)
ESCHAR ( 1 FDA reports)
EXTRADURAL ABSCESS ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVECTOMY ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEAT STROKE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATITIS C ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERPHOSPHATASAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOSPADIAS ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
ICHTHYOSIS ( 1 FDA reports)
ILEUS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPLANT SITE EFFUSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTION SUSCEPTIBILITY INCREASED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL SELF-INJURY ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARGE INTESTINE CARCINOMA ( 1 FDA reports)
LENS DISORDER ( 1 FDA reports)
LENTICULAR OPACITIES ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MEDICAL DIET ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MEGACOLON ( 1 FDA reports)
MENINGEOMAS SURGERY ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASES TO NERVOUS SYSTEM ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO ADVERSE EFFECT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
ONYCHOMYCOSIS ( 1 FDA reports)
OPTIC DISC DISORDER ( 1 FDA reports)
OPTIC NERVE DISORDER ( 1 FDA reports)
ORAL MUCOSAL ERUPTION ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLEURAL HAEMORRHAGE ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
PORIOMANIA ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
PORPHYRINS URINE INCREASED ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
POSTOPERATIVE INFECTION ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
POTENTIATING DRUG INTERACTION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROPOFOL INFUSION SYNDROME ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
RELAPSING-REMITTING MULTIPLE SCLEROSIS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL TUBULAR ATROPHY ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RETICULOCYTOPENIA ( 1 FDA reports)
RETINITIS ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCAR ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SMALL INTESTINAL PERFORATION ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPLEEN SCAN ABNORMAL ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TIC ( 1 FDA reports)
TINEA INFECTION ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TOXIC INDUCED ENCEPHALOPATHY ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
ULCER ( 1 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETHRAL INJURY ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VIRAL LOAD INCREASED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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