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

CONFUSIONAL STATE ( 42 FDA reports)
RENAL FAILURE ( 37 FDA reports)
MALAISE ( 35 FDA reports)
RENAL FAILURE ACUTE ( 26 FDA reports)
DRUG INTERACTION ( 24 FDA reports)
THROMBOCYTOPENIA ( 23 FDA reports)
BRADYCARDIA ( 22 FDA reports)
HYPONATRAEMIA ( 22 FDA reports)
COMA ( 21 FDA reports)
DIARRHOEA ( 21 FDA reports)
FALL ( 21 FDA reports)
DYSPNOEA ( 20 FDA reports)
PYREXIA ( 19 FDA reports)
ANAEMIA ( 18 FDA reports)
ASTHENIA ( 18 FDA reports)
CYTOLYTIC HEPATITIS ( 18 FDA reports)
MYALGIA ( 18 FDA reports)
VOMITING ( 18 FDA reports)
ARTHRALGIA ( 17 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 17 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 17 FDA reports)
OEDEMA PERIPHERAL ( 17 FDA reports)
HYPERTENSION ( 16 FDA reports)
HYPOTENSION ( 15 FDA reports)
NEUTROPENIA ( 15 FDA reports)
RASH MACULO-PAPULAR ( 15 FDA reports)
HEADACHE ( 14 FDA reports)
PANCYTOPENIA ( 14 FDA reports)
ENCEPHALOPATHY ( 13 FDA reports)
HYPOGLYCAEMIA ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
OVERDOSE ( 13 FDA reports)
CHOLESTASIS ( 12 FDA reports)
DISORIENTATION ( 12 FDA reports)
ERYTHEMA ( 12 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 12 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 12 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
HEPATIC CIRRHOSIS ( 11 FDA reports)
NAUSEA ( 11 FDA reports)
ODYNOPHAGIA ( 11 FDA reports)
PAIN ( 11 FDA reports)
PORTAL VEIN THROMBOSIS ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
SOMNOLENCE ( 11 FDA reports)
TREMOR ( 11 FDA reports)
URTICARIA ( 11 FDA reports)
ANAPHYLACTIC SHOCK ( 10 FDA reports)
BONE PAIN ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
CONJUNCTIVITIS ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 10 FDA reports)
HAEMATOMA ( 10 FDA reports)
LUNG DISORDER ( 10 FDA reports)
PANCREATITIS ACUTE ( 10 FDA reports)
STEVENS-JOHNSON SYNDROME ( 10 FDA reports)
ABORTION INDUCED ( 9 FDA reports)
CHEST PAIN ( 9 FDA reports)
ESCHERICHIA SEPSIS ( 9 FDA reports)
HALLUCINATION ( 9 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 9 FDA reports)
OLIGOHYDRAMNIOS ( 9 FDA reports)
PARAESTHESIA ( 9 FDA reports)
PURPURA ( 9 FDA reports)
RHABDOMYOLYSIS ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
AGRANULOCYTOSIS ( 8 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
DERMATITIS EXFOLIATIVE ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 8 FDA reports)
HEPATIC FAILURE ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
HYPERURICAEMIA ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
ABDOMINAL PAIN ( 7 FDA reports)
ACUTE PULMONARY OEDEMA ( 7 FDA reports)
ANOREXIA ( 7 FDA reports)
ARTHRITIS ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
EOSINOPHILIA ( 7 FDA reports)
FOETAL GROWTH RETARDATION ( 7 FDA reports)
HEPATITIS CHOLESTATIC ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
INFLAMMATION ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
PULMONARY OEDEMA ( 7 FDA reports)
RASH ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ABDOMINAL PAIN UPPER ( 6 FDA reports)
AGITATION ( 6 FDA reports)
ASCITES ( 6 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BLOOD CREATININE INCREASED ( 6 FDA reports)
CARDIAC FAILURE ( 6 FDA reports)
CEREBELLAR SYNDROME ( 6 FDA reports)
CIRCULATORY COLLAPSE ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DEATH ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
FOETAL MOVEMENTS DECREASED ( 6 FDA reports)
HYPERSENSITIVITY ( 6 FDA reports)
HYPERTHERMIA ( 6 FDA reports)
HYPOCALCAEMIA ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
JOINT EFFUSION ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
MIGRAINE ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PYELONEPHRITIS ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
TRANSAMINASES INCREASED ( 6 FDA reports)
VISUAL DISTURBANCE ( 6 FDA reports)
ALOPECIA ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 5 FDA reports)
CARDIOGENIC SHOCK ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CORONARY ARTERY INSUFFICIENCY ( 5 FDA reports)
DIPLOPIA ( 5 FDA reports)
DYSPEPSIA ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
FEMORAL NECK FRACTURE ( 5 FDA reports)
HAEMODYNAMIC INSTABILITY ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPERTHYROIDISM ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
MULTI-ORGAN FAILURE ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
ORAL MUCOSAL ERUPTION ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SHOCK ( 5 FDA reports)
SQUAMOUS CELL CARCINOMA ( 5 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
TOXIC SKIN ERUPTION ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
VISUAL ACUITY REDUCED ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 4 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 4 FDA reports)
BLOOD GLUCOSE INCREASED ( 4 FDA reports)
BRONCHOSPASM ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
COGNITIVE DISORDER ( 4 FDA reports)
COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS ( 4 FDA reports)
COUGH ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
DERMATITIS BULLOUS ( 4 FDA reports)
EOSINOPHIL COUNT DECREASED ( 4 FDA reports)
EYELID OEDEMA ( 4 FDA reports)
FACIAL NEURALGIA ( 4 FDA reports)
GLARE ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HEART RATE DECREASED ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATOMEGALY ( 4 FDA reports)
HYPERCHOLESTEROLAEMIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
INTENTIONAL OVERDOSE ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
MYDRIASIS ( 4 FDA reports)
NEONATAL DISORDER ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
ORTHOSTATIC HYPOTENSION ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PLACENTAL DISORDER ( 4 FDA reports)
PLACENTAL INSUFFICIENCY ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 4 FDA reports)
RALES ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
STAPHYLOCOCCAL INFECTION ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
WALKING AID USER ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 3 FDA reports)
ANAEMIA MACROCYTIC ( 3 FDA reports)
ANAPHYLACTOID REACTION ( 3 FDA reports)
ANGIOEDEMA ( 3 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES POSITIVE ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ASTERIXIS ( 3 FDA reports)
AUTOIMMUNE THYROIDITIS ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CELL DEATH ( 3 FDA reports)
COAGULOPATHY ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 3 FDA reports)
ENTEROBACTER SEPSIS ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FOETAL DISORDER ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HEPATIC STEATOSIS ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPERAMMONAEMIA ( 3 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 3 FDA reports)
HYPOALBUMINAEMIA ( 3 FDA reports)
INFECTION ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LYMPHOCYTOSIS ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PARKINSONISM ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PETIT MAL EPILEPSY ( 3 FDA reports)
PHLEBITIS ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
PREMATURE BABY ( 3 FDA reports)
PRODUCTIVE COUGH ( 3 FDA reports)
PROSTATE CANCER ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RESPIRATORY ALKALOSIS ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SERUM SICKNESS ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SLEEP WALKING ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
STATUS EPILEPTICUS ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TORSADE DE POINTES ( 3 FDA reports)
ULTRASOUND ABDOMEN ABNORMAL ( 3 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 3 FDA reports)
VARICES OESOPHAGEAL ( 3 FDA reports)
VISUAL FIELD DEFECT ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
AFFECTIVE DISORDER ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
AMMONIA INCREASED ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANOXIC ENCEPHALOPATHY ( 2 FDA reports)
AORTIC BYPASS ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ASPERGILLOSIS ( 2 FDA reports)
ASPIRATION BRONCHIAL ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 2 FDA reports)
BLOOD HOMOCYSTEINE INCREASED ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BREECH PRESENTATION ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BRONCHOPNEUMOPATHY ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CAPILLARY LEAK SYNDROME ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 125 INCREASED ( 2 FDA reports)
CARBOHYDRATE ANTIGEN 19-9 INCREASED ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CATHETER RELATED INFECTION ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CEREBRAL DISORDER ( 2 FDA reports)
CEREBRAL ISCHAEMIA ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
COGWHEEL RIGIDITY ( 2 FDA reports)
CONGENITAL ANOMALY ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECZEMA ASTEATOTIC ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ENDOMETRIOSIS ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ENTEROBACTER INFECTION ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ESCHERICHIA INFECTION ( 2 FDA reports)
EXTRASYSTOLES ( 2 FDA reports)
FACIAL DYSMORPHISM ( 2 FDA reports)
FACIAL PALSY ( 2 FDA reports)
FALLOT'S TETRALOGY ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
FOETAL DISTRESS SYNDROME ( 2 FDA reports)
FOETOR HEPATICUS ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC PERFORATION ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GASTROSTOMY TUBE INSERTION ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED ERYTHEMA ( 2 FDA reports)
GINGIVAL BLEEDING ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HAEMOTHORAX ( 2 FDA reports)
HELLP SYNDROME ( 2 FDA reports)
HEMIPLEGIA ( 2 FDA reports)
HEPATIC LESION ( 2 FDA reports)
HEPATIC NEOPLASM ( 2 FDA reports)
HEPATORENAL SYNDROME ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERGAMMAGLOBULINAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOREFLEXIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOVENTILATION NEONATAL ( 2 FDA reports)
HYPOVOLAEMIC SHOCK ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IATROGENIC INJURY ( 2 FDA reports)
IMPAIRED SELF-CARE ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INTRACARDIAC THROMBUS ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
IVTH NERVE PARALYSIS ( 2 FDA reports)
KLEBSIELLA SEPSIS ( 2 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 2 FDA reports)
LIP OEDEMA ( 2 FDA reports)
LOCALISED OEDEMA ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
MEDIASTINAL DISORDER ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MENINGITIS ENTEROVIRAL ( 2 FDA reports)
MESENTERIC VEIN THROMBOSIS ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHIL PERCENTAGE DECREASED ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NOSOCOMIAL INFECTION ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OSTEONECROSIS OF JAW ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARAKERATOSIS ( 2 FDA reports)
PAROXYSMAL ARRHYTHMIA ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLASMACYTOSIS ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
PORPHYRIA NON-ACUTE ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PROCEDURAL COMPLICATION ( 2 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 2 FDA reports)
PRURIGO ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PSYCHOMOTOR SKILLS IMPAIRED ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL APLASIA ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
RESUSCITATION ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUS ARRHYTHMIA ( 2 FDA reports)
SINUS BRADYCARDIA ( 2 FDA reports)
SKIN TEST NEGATIVE ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SPINAL FUSION ACQUIRED ( 2 FDA reports)
SPINAL MYELOGRAM ABNORMAL ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRESS SYMPTOMS ( 2 FDA reports)
TALIPES ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
TOE AMPUTATION ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
ULTRASOUND ANTENATAL SCREEN ABNORMAL ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
URTICARIA PAPULAR ( 2 FDA reports)
VAGUS NERVE DISORDER ( 2 FDA reports)
VASODILATATION ( 2 FDA reports)
VENOUS THROMBOSIS LIMB ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABDOMINAL WALL HAEMORRHAGE ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACQUIRED CARDIAC SEPTAL DEFECT ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AIDS ENCEPHALOPATHY ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALCOHOL PROBLEM ( 1 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 1 FDA reports)
ALVEOLITIS ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANOSOGNOSIA ( 1 FDA reports)
ANTEROGRADE AMNESIA ( 1 FDA reports)
ANTIBODY TEST ABNORMAL ( 1 FDA reports)
ANTIBODY TEST POSITIVE ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APHONIA PSYCHOGENIC ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPARENT DEATH ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL HAEMORRHAGE ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERY DISSECTION ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AUTOANTIBODY POSITIVE ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
AZOOSPERMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERASCITES ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BETA GLOBULIN INCREASED ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GASES ABNORMAL ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IRON INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD UREA DECREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BONE MARROW TOXICITY ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHIOLITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CAPILLARY NAIL REFILL TEST ( 1 FDA reports)
CARBON MONOXIDE DIFFUSING CAPACITY DECREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVICAL ROOT PAIN ( 1 FDA reports)
CERVICAL VERTEBRAL FRACTURE ( 1 FDA reports)
CERVIX DISORDER ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 1 FDA reports)
CIRRHOSIS ALCOHOLIC ( 1 FDA reports)
CLONUS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ( 1 FDA reports)
COMPLEMENT FACTOR INCREASED ( 1 FDA reports)
COMPULSIVE SHOPPING ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL NOSE MALFORMATION ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CSF PROTEIN INCREASED ( 1 FDA reports)
CYST ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS NEUROSENSORY ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM FEBRILE ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSIONAL DISORDER, UNSPECIFIED TYPE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG NAME CONFUSION ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG WITHDRAWAL HEADACHE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR MALFORMATION ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ECHOGRAPHY ABNORMAL ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EHLERS-DANLOS SYNDROME ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ELECTROMYOGRAM ABNORMAL ( 1 FDA reports)
EMBOLISM ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPHYSEMATOUS CYSTITIS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
EOSINOPHILIC COLITIS ( 1 FDA reports)
EPICONDYLITIS ( 1 FDA reports)
EPISCLERITIS ( 1 FDA reports)
EROSIVE DUODENITIS ( 1 FDA reports)
ERYTHEMA NODOSUM ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
FACIAL BONES FRACTURE ( 1 FDA reports)
FACTOR II DEFICIENCY ( 1 FDA reports)
FIBROMUSCULAR DYSPLASIA ( 1 FDA reports)
FLUID REPLACEMENT ( 1 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC ULCER PERFORATION ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GROWTH RETARDATION ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHOID OPERATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HENOCH-SCHONLEIN PURPURA ( 1 FDA reports)
HEPATIC ENZYME ABNORMAL ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOCELLULAR INJURY ( 1 FDA reports)
HEPATOJUGULAR REFLUX ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HOLMES-ADIE PUPIL ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERPROTEINAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTONIA NEONATAL ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOTONIA NEONATAL ( 1 FDA reports)
ILIAC ARTERY THROMBOSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFANTILE COLIC ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JC VIRUS INFECTION ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
KETONURIA ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARGE INTESTINAL ULCER ( 1 FDA reports)
LARYNGEAL OBSTRUCTION ( 1 FDA reports)
LEFT VENTRICULAR END-DIASTOLIC PRESSURE INCREASED ( 1 FDA reports)
LIFE SUPPORT ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LYMPH NODES SCAN ABNORMAL ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARFAN'S SYNDROME ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MECHANICAL COMPLICATION OF IMPLANT ( 1 FDA reports)
MECONIUM IN AMNIOTIC FLUID ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MONARTHRITIS ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE CONTRACTURE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYCOSIS FUNGOIDES ( 1 FDA reports)
MYCOTIC ANEURYSM ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NEONATAL THYROTOXICOSIS ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NERVE ROOT COMPRESSION ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NOCTURNAL DYSPNOEA ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OESOPHAGEAL VARICES HAEMORRHAGE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OSTEITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OSTEOTOMY ( 1 FDA reports)
PALATAL OEDEMA ( 1 FDA reports)
PALLANAESTHESIA ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PELVIC FRACTURE ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PHOTOPSIA ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLACENTAL INFARCTION ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
PORTAL HYPERTENSION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PRINZMETAL ANGINA ( 1 FDA reports)
PROCTITIS ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PROTHROMBIN TIME RATIO INCREASED ( 1 FDA reports)
PRURITUS ALLERGIC ( 1 FDA reports)
PSEUDOLYMPHOMA ( 1 FDA reports)
PSITTACOSIS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
RADIAL PULSE ABNORMAL ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RENAL CANCER ( 1 FDA reports)
RENAL HYPOPLASIA ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENIN INCREASED ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION BACTERIAL ( 1 FDA reports)
RETROGRADE AMNESIA ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEXUAL DYSFUNCTION ( 1 FDA reports)
SIGMOIDITIS ( 1 FDA reports)
SIMPLE PARTIAL SEIZURES ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN PLAQUE ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYPHILIS ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THOUGHT BLOCKING ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE CANCER METASTATIC ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOXIC NODULAR GOITRE ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VISUAL PATHWAY DISORDER ( 1 FDA reports)
VITAL CAPACITY DECREASED ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITH NERVE PARALYSIS ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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