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

PLATELET COUNT DECREASED ( 33 FDA reports)
ANAEMIA ( 27 FDA reports)
CARDIAC FAILURE ( 27 FDA reports)
INTERSTITIAL LUNG DISEASE ( 26 FDA reports)
HYPOKALAEMIA ( 25 FDA reports)
PNEUMONIA ( 24 FDA reports)
SEPSIS ( 22 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 21 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 20 FDA reports)
BRONCHITIS ( 20 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 19 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 19 FDA reports)
LIVER DISORDER ( 19 FDA reports)
DIARRHOEA ( 17 FDA reports)
PYREXIA ( 16 FDA reports)
BLOOD PRESSURE DECREASED ( 15 FDA reports)
NAUSEA ( 15 FDA reports)
CONDITION AGGRAVATED ( 14 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 14 FDA reports)
DRUG INEFFECTIVE ( 14 FDA reports)
FEBRILE NEUTROPENIA ( 14 FDA reports)
RHABDOMYOLYSIS ( 14 FDA reports)
ABDOMINAL PAIN ( 13 FDA reports)
BLOOD CREATININE INCREASED ( 13 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
DECREASED APPETITE ( 13 FDA reports)
MALAISE ( 13 FDA reports)
RENAL FAILURE ( 13 FDA reports)
DEHYDRATION ( 12 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 12 FDA reports)
HAEMOGLOBIN DECREASED ( 12 FDA reports)
RASH ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
CARDIAC ARREST ( 11 FDA reports)
FALL ( 11 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 11 FDA reports)
MELAENA ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
RHEUMATOID ARTHRITIS ( 11 FDA reports)
ABNORMAL BEHAVIOUR ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
SHOCK ( 10 FDA reports)
ANOREXIA ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
BLOOD POTASSIUM DECREASED ( 9 FDA reports)
ERYTHEMA MULTIFORME ( 9 FDA reports)
HEPATIC ENCEPHALOPATHY ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
SKIN ULCER ( 9 FDA reports)
VOMITING ( 9 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
HYPERTENSION ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
TACHYCARDIA ( 8 FDA reports)
AUTOIMMUNE THYROIDITIS ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 7 FDA reports)
CARDIO-RESPIRATORY ARREST ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 7 FDA reports)
HYPERKALAEMIA ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
THYROID DISORDER ( 7 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 7 FDA reports)
ANAEMIA NEONATAL ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CIRCULATORY FAILURE NEONATAL ( 6 FDA reports)
DECREASED ACTIVITY ( 6 FDA reports)
DRUG ERUPTION ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
DYSPNOEA EXERTIONAL ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 6 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 6 FDA reports)
GLAUCOMA ( 6 FDA reports)
HAEMATOCRIT DECREASED ( 6 FDA reports)
INTESTINAL OBSTRUCTION ( 6 FDA reports)
LOW BIRTH WEIGHT BABY ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
PNEUMOTHORAX ( 6 FDA reports)
PREMATURE BABY ( 6 FDA reports)
SKIN INFECTION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
VISUAL ACUITY REDUCED ( 6 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ARRHYTHMIA ( 5 FDA reports)
BLOOD CHLORIDE DECREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD SODIUM DECREASED ( 5 FDA reports)
BREAST CANCER RECURRENT ( 5 FDA reports)
BRONCHOSPASM ( 5 FDA reports)
CATHETER RELATED INFECTION ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
EATING DISORDER ( 5 FDA reports)
EOSINOPHIL COUNT INCREASED ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
IRON DEFICIENCY ANAEMIA ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 5 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 5 FDA reports)
NEUTROPENIA ( 5 FDA reports)
OVARIAN CANCER ( 5 FDA reports)
PERIPHERAL COLDNESS ( 5 FDA reports)
PRIMARY HYPERALDOSTERONISM ( 5 FDA reports)
PULMONARY HAEMORRHAGE ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
AUTOIMMUNE HEPATITIS ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BONE MARROW FAILURE ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 4 FDA reports)
COUGH ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GYNAECOMASTIA ( 4 FDA reports)
HEPATIC NECROSIS ( 4 FDA reports)
HEPATITIS C ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPERAMMONAEMIA ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
INTRACARDIAC THROMBUS ( 4 FDA reports)
LACTIC ACIDOSIS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NO ADVERSE EVENT ( 4 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 4 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 4 FDA reports)
OFF LABEL USE ( 4 FDA reports)
PAIN ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PLEURAL EFFUSION ( 4 FDA reports)
PO2 DECREASED ( 4 FDA reports)
RIGHT VENTRICULAR FAILURE ( 4 FDA reports)
SPINAL COMPRESSION FRACTURE ( 4 FDA reports)
STEVENS-JOHNSON SYNDROME ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TREMOR ( 4 FDA reports)
VENA CAVA THROMBOSIS ( 4 FDA reports)
VITREOUS HAEMORRHAGE ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ADENOCARCINOMA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ASPIRATION ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 3 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
CARDIOGENIC SHOCK ( 3 FDA reports)
CLAVICLE FRACTURE ( 3 FDA reports)
COMA ( 3 FDA reports)
CONVULSION ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
EYE HAEMORRHAGE ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FUNGAL SEPSIS ( 3 FDA reports)
GASTRITIS HAEMORRHAGIC ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GENERALISED ERYTHEMA ( 3 FDA reports)
GRIP STRENGTH DECREASED ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOCHROMIC ANAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA NEONATAL ( 3 FDA reports)
HYPOXIA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
LUNG ABSCESS ( 3 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 3 FDA reports)
MALIGNANT ASCITES ( 3 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCLE TWITCHING ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYOCARDIAL FIBROSIS ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
MYOCARDITIS ( 3 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OCULAR HYPERTENSION ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
PROTEIN TOTAL DECREASED ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PULMONARY HYPOPLASIA ( 3 FDA reports)
PUPILLARY LIGHT REFLEX TESTS ABNORMAL ( 3 FDA reports)
PYODERMA ( 3 FDA reports)
RENAL FAILURE NEONATAL ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESTLESSNESS ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 3 FDA reports)
ABDOMINAL ADHESIONS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANAL CANCER ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANOSMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD URIC ACID INCREASED ( 2 FDA reports)
BONE MARROW DISORDER ( 2 FDA reports)
BRADYARRHYTHMIA ( 2 FDA reports)
BRAIN HERNIATION ( 2 FDA reports)
BRAIN OEDEMA ( 2 FDA reports)
BREAST MASS ( 2 FDA reports)
BREAST PAIN ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLANGITIS SUPPURATIVE ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT SHORTENED ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 2 FDA reports)
ENCEPHALITIS FUNGAL ( 2 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 2 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HUMAN HERPES VIRUS 6 SEROLOGY POSITIVE ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERPHOSPHATAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILIAC ARTERY THROMBOSIS ( 2 FDA reports)
IMMOBILE ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 2 FDA reports)
IRON DEFICIENCY ( 2 FDA reports)
LIPASE INCREASED ( 2 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MARASMUS ( 2 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METASTASES TO LYMPH NODES ( 2 FDA reports)
MONOCYTE COUNT DECREASED ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MYELOBLAST COUNT INCREASED ( 2 FDA reports)
MYELOCYTE COUNT DECREASED ( 2 FDA reports)
NEONATAL ASPHYXIA ( 2 FDA reports)
NEPHROGENIC ANAEMIA ( 2 FDA reports)
OLIGOHYDRAMNIOS ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL MUCOSAL ERUPTION ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANCREATITIS ACUTE ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PHANTOM PAIN ( 2 FDA reports)
PLATELET COUNT NORMAL ( 2 FDA reports)
PNEUMONIA ASPIRATION ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
POVERTY OF SPEECH ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PURPURA ( 2 FDA reports)
PYODERMA GANGRENOSUM ( 2 FDA reports)
QRS AXIS ABNORMAL ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RESPIRATORY ALKALOSIS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUPERINFECTION ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TRABECULECTOMY ( 2 FDA reports)
TUBERCULOUS PLEURISY ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VIRAL MYOCARDITIS ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL CHEST SOUND ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADHESION ( 1 FDA reports)
ADRENALECTOMY ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AMPUTATION ( 1 FDA reports)
ANAL FISTULA ( 1 FDA reports)
ANAL STENOSIS ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANORECTAL DISORDER ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPHYXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACTERIAL DIARRHOEA ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASEDOW'S DISEASE ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALDOSTERONE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BURSITIS INFECTIVE ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDA SEPSIS ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
COMPUTERISED TOMOGRAM NORMAL ( 1 FDA reports)
CORNEAL EROSION ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
DELUSIONAL DISORDER, EROTOMANIC TYPE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIZZINESS ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLIC STROKE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROCOLITIS BACTERIAL ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYELID EROSION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEEDING DISORDER NEONATAL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL DISTRESS SYNDROME ( 1 FDA reports)
FOETAL GROWTH RETARDATION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GLAUCOMA SURGERY ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLUCOSE URINE PRESENT ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEAD BANGING ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNAL HERNIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JEJUNAL PERFORATION ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALABSORPTION ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL CONDITION AFFECTING FOETUS ( 1 FDA reports)
MECONIUM STAIN ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO CHEST WALL ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYELITIS TRANSVERSE ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NEONATAL HYPONATRAEMIA ( 1 FDA reports)
NEONATAL HYPOTENSION ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OEDEMA GENITAL ( 1 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OVARIAN EPITHELIAL CANCER ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PERIPHERAL OEDEMA NEONATAL ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 1 FDA reports)
PNEUMATOSIS INTESTINALIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA FUNGAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RALES ( 1 FDA reports)
RECTOSIGMOID CANCER ( 1 FDA reports)
REGURGITATION ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RETINAL VEIN OCCLUSION ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SERUM SICKNESS ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THIRST ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TRAUMATIC SHOCK ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)

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