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

PYREXIA ( 55 FDA reports)
MALAISE ( 31 FDA reports)
NAUSEA ( 28 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 27 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 27 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 26 FDA reports)
INTERSTITIAL LUNG DISEASE ( 25 FDA reports)
PNEUMONIA ( 25 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 23 FDA reports)
ANAEMIA ( 22 FDA reports)
PLATELET COUNT DECREASED ( 21 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 20 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 19 FDA reports)
SPEECH DISORDER ( 19 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 18 FDA reports)
DIARRHOEA ( 18 FDA reports)
DIZZINESS ( 18 FDA reports)
HYPONATRAEMIA ( 18 FDA reports)
VOMITING ( 18 FDA reports)
BLOOD UREA INCREASED ( 17 FDA reports)
HAEMOGLOBIN DECREASED ( 17 FDA reports)
RENAL FAILURE ACUTE ( 16 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 16 FDA reports)
ERYTHEMA ( 15 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 15 FDA reports)
PAIN ( 15 FDA reports)
TREMOR ( 15 FDA reports)
BLOOD SODIUM DECREASED ( 14 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 14 FDA reports)
BLOOD CREATININE INCREASED ( 13 FDA reports)
CONDITION AGGRAVATED ( 13 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
INSOMNIA ( 13 FDA reports)
LIVER DISORDER ( 13 FDA reports)
LOSS OF CONSCIOUSNESS ( 13 FDA reports)
OSTEONECROSIS ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
SWELLING ( 13 FDA reports)
ANOREXIA ( 12 FDA reports)
ARTHRALGIA ( 12 FDA reports)
DELIRIUM ( 12 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 12 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 12 FDA reports)
NEPHROTIC SYNDROME ( 12 FDA reports)
RASH ( 12 FDA reports)
RESPIRATORY FAILURE ( 12 FDA reports)
SOMNOLENCE ( 12 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 12 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
DEATH ( 11 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 11 FDA reports)
NEUTROPENIA ( 11 FDA reports)
AGRANULOCYTOSIS ( 10 FDA reports)
BACTERIAL INFECTION ( 10 FDA reports)
BONE DISORDER ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
CHILLS ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
DECREASED APPETITE ( 10 FDA reports)
DYSPNOEA ( 10 FDA reports)
GINGIVITIS ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
TOOTH EXTRACTION ( 10 FDA reports)
ABDOMINAL PAIN UPPER ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
CARDIAC FAILURE ( 9 FDA reports)
DYSPHAGIA ( 9 FDA reports)
HAEMATOCRIT DECREASED ( 9 FDA reports)
HYPOAESTHESIA ( 9 FDA reports)
HYPOKALAEMIA ( 9 FDA reports)
PNEUMOTHORAX ( 9 FDA reports)
PRODUCTIVE COUGH ( 9 FDA reports)
PULMONARY FIBROSIS ( 9 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 9 FDA reports)
RENAL DISORDER ( 9 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
COUGH ( 8 FDA reports)
DISEASE PROGRESSION ( 8 FDA reports)
DRUG ERUPTION ( 8 FDA reports)
DYSSTASIA ( 8 FDA reports)
ENCEPHALOPATHY ( 8 FDA reports)
EYELID OEDEMA ( 8 FDA reports)
FEELING ABNORMAL ( 8 FDA reports)
HYPERGLYCAEMIA ( 8 FDA reports)
IMPAIRED HEALING ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
PLEURAL EFFUSION ( 8 FDA reports)
RESTLESSNESS ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
SHOCK ( 8 FDA reports)
THROMBOTIC STROKE ( 8 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BLOOD PRESSURE INCREASED ( 7 FDA reports)
DEHYDRATION ( 7 FDA reports)
DENTAL CARE ( 7 FDA reports)
DYSLALIA ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
HYPOXIA ( 7 FDA reports)
MYOCARDIAL INFARCTION ( 7 FDA reports)
OXYGEN SATURATION DECREASED ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
PNEUMONIA ASPIRATION ( 7 FDA reports)
PRIMARY SEQUESTRUM ( 7 FDA reports)
RASH GENERALISED ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
SEQUESTRECTOMY ( 7 FDA reports)
TALIPES ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
TOOTHACHE ( 7 FDA reports)
WOUND CLOSURE ( 7 FDA reports)
WOUND SECRETION ( 7 FDA reports)
X-RAY ABNORMAL ( 7 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 6 FDA reports)
BLISTER ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
COMMUNICATION DISORDER ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
DRUG INTERACTION ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
DYSURIA ( 6 FDA reports)
ERYTHEMA MULTIFORME ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
MUSCLE TIGHTNESS ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
ORAL PAIN ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ANGINA PECTORIS ( 5 FDA reports)
BLOOD BILIRUBIN INCREASED ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
BRAIN DEATH ( 5 FDA reports)
BRAIN OEDEMA ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CEREBRAL HAEMORRHAGE ( 5 FDA reports)
DRY SKIN ( 5 FDA reports)
FAECES DISCOLOURED ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 5 FDA reports)
HEMIPARESIS ( 5 FDA reports)
HEPATIC CIRRHOSIS ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
HYPOKINESIA ( 5 FDA reports)
INFECTION ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
LYMPHOCYTIC INFILTRATION ( 5 FDA reports)
MOUTH HAEMORRHAGE ( 5 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 5 FDA reports)
OSTEOPOROSIS ( 5 FDA reports)
PLATELET COUNT INCREASED ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
STUPOR ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
WEIGHT INCREASED ( 5 FDA reports)
AMNESIA ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
ARTERIOSCLEROSIS ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BILE DUCT STONE ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CHOLANGITIS ACUTE ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
DEBRIDEMENT ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
EOSINOPHIL COUNT INCREASED ( 4 FDA reports)
ESSENTIAL THROMBOCYTHAEMIA ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HEAD DISCOMFORT ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
INDURATION ( 4 FDA reports)
INTRACRANIAL TUMOUR HAEMORRHAGE ( 4 FDA reports)
LOBAR PNEUMONIA ( 4 FDA reports)
MYASTHENIA GRAVIS ( 4 FDA reports)
NECROSIS ( 4 FDA reports)
ORGANISING PNEUMONIA ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PERONEAL NERVE PALSY ( 4 FDA reports)
QUADRIPLEGIA ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
RESPIRATORY TRACT OEDEMA ( 4 FDA reports)
SINUS TACHYCARDIA ( 4 FDA reports)
STOMACH DISCOMFORT ( 4 FDA reports)
SUDDEN DEATH ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
AFFECT LABILITY ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
APALLIC SYNDROME ( 3 FDA reports)
APLASIA PURE RED CELL ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BLOOD URINE PRESENT ( 3 FDA reports)
BLUNTED AFFECT ( 3 FDA reports)
BRAIN STEM INFARCTION ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 3 FDA reports)
CARDIAC HYPERTROPHY ( 3 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
CHRONIC SINUSITIS ( 3 FDA reports)
COLITIS ( 3 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DIABETES INSIPIDUS ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DUODENAL ULCER ( 3 FDA reports)
EOSINOPHILIC PNEUMONIA ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FALL ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GENITAL HAEMORRHAGE ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
HERPES SIMPLEX ( 3 FDA reports)
HERPES ZOSTER ( 3 FDA reports)
HODGKIN'S DISEASE ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
ILEUS ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MULTIPLE MYELOMA ( 3 FDA reports)
MUSCLE RIGIDITY ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OSTEONECROSIS OF JAW ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PANCREATITIS ACUTE ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PURPURA ( 3 FDA reports)
RENAL ATROPHY ( 3 FDA reports)
RENAL HYPERTROPHY ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RETINAL EXUDATES ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
TENDERNESS ( 3 FDA reports)
THERAPEUTIC PROCEDURE ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TONGUE NEOPLASM MALIGNANT STAGE UNSPECIFIED ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
WOUND DEBRIDEMENT ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ANTITHROMBIN III DECREASED ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLUE TOE SYNDROME ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BREAST ADENOMA ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CAROTID ARTERIOSCLEROSIS ( 2 FDA reports)
CEREBRAL ARTERY STENOSIS ( 2 FDA reports)
CERVICOBRACHIAL SYNDROME ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DERMATITIS ALLERGIC ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIFFUSE ALVEOLAR DAMAGE ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
EMBOLISM ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
EYE MOVEMENT DISORDER ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FAT EMBOLISM ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTRODUODENAL ULCER ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATITIS FULMINANT ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HODGKIN'S DISEASE STAGE IV ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERAMMONAEMIA ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOPROTEINAEMIA ( 2 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INTRACRANIAL ANEURYSM ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LACUNAR INFARCTION ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MENINGITIS ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 2 FDA reports)
MUSCLE CONTRACTURE ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUTROPHIL COUNT INCREASED ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OPPORTUNISTIC INFECTION ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 2 FDA reports)
PANCREATIC DISORDER ( 2 FDA reports)
PANCREATOLITHIASIS ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERIARTHRITIS ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIODONTITIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
PNEUMONIA LEGIONELLA ( 2 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 2 FDA reports)
PRESCRIBED OVERDOSE ( 2 FDA reports)
PROTEIN TOTAL ABNORMAL ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PRURITUS ALLERGIC ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULMONARY THROMBOSIS ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RESPIRATORY TRACT INFECTION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SPINAL COMPRESSION FRACTURE ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUBDURAL HAEMATOMA ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
TUMOUR EXCISION ( 2 FDA reports)
URETERIC CANCER ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABSCESS ORAL ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOMONOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALOPECIA AREATA ( 1 FDA reports)
ALPHA 1 FOETOPROTEIN INCREASED ( 1 FDA reports)
ANAESTHETIC COMPLICATION ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTINEUTROPHIL CYTOPLASMIC ANTIBODY ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASCITES ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AUTOIMMUNE HEPATITIS ( 1 FDA reports)
BACILLUS INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BRONCHITIS ACUTE ( 1 FDA reports)
BRONCHOGRAM ABNORMAL ( 1 FDA reports)
CANDIDA SEROLOGY POSITIVE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CATHETER PLACEMENT ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVAL EROSION ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG RESISTANCE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
FLASHBACK ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC HYPERMOTILITY ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GASTROINTESTINAL FISTULA ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMOCONCENTRATION ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAND DEFORMITY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ATROPHY ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATORY MARKER INCREASED ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERVERTEBRAL DISCITIS ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LAPAROSCOPIC SURGERY ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIVER CARCINOMA RUPTURED ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LUNG ADENOCARCINOMA STAGE IV ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INJURY ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
METASTASES TO BREAST ( 1 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE ABSCESS ( 1 FDA reports)
MUSCLE SWELLING ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NEUROSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PAPILLARY THYROID CANCER ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PARTNER STRESS ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PHARYNGEAL ABSCESS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHARYNX DISCOMFORT ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURAL ADHESION ( 1 FDA reports)
PNEUMOCYSTIS CARINII PNEUMONIA ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
PORPHYRIA NON-ACUTE ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SWEAT DISCOLOURATION ( 1 FDA reports)
SYNOVIAL CYST ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
THIRST ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 1 FDA reports)
URETERIC STENOSIS ( 1 FDA reports)
URINARY OCCULT BLOOD POSITIVE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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