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

NAUSEA ( 32 FDA reports)
DEATH ( 31 FDA reports)
DIARRHOEA ( 31 FDA reports)
PYREXIA ( 31 FDA reports)
DYSPNOEA ( 25 FDA reports)
PNEUMONIA ( 24 FDA reports)
FATIGUE ( 23 FDA reports)
MALAISE ( 23 FDA reports)
DIZZINESS ( 21 FDA reports)
CEREBROVASCULAR ACCIDENT ( 20 FDA reports)
VOMITING ( 20 FDA reports)
DEHYDRATION ( 18 FDA reports)
FALL ( 17 FDA reports)
PRURITUS ( 17 FDA reports)
MYOCARDIAL INFARCTION ( 16 FDA reports)
PULMONARY EMBOLISM ( 16 FDA reports)
CIRCULATORY COLLAPSE ( 15 FDA reports)
THROMBOCYTOPENIA ( 15 FDA reports)
WEIGHT DECREASED ( 15 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 14 FDA reports)
PAIN ( 14 FDA reports)
RENAL FAILURE ( 14 FDA reports)
CONSTIPATION ( 13 FDA reports)
MULTI-ORGAN FAILURE ( 13 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 13 FDA reports)
URINARY TRACT INFECTION ( 13 FDA reports)
UROSEPSIS ( 13 FDA reports)
HEADACHE ( 11 FDA reports)
HYPERSENSITIVITY ( 11 FDA reports)
HYPOTENSION ( 11 FDA reports)
BRADYCARDIA ( 10 FDA reports)
CARDIAC FAILURE ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
BLOOD PRESSURE INCREASED ( 9 FDA reports)
BONE PAIN ( 9 FDA reports)
CONDITION AGGRAVATED ( 9 FDA reports)
DEPRESSION ( 9 FDA reports)
RASH ( 9 FDA reports)
SEPSIS ( 9 FDA reports)
ASTHENIA ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HEPATITIS TOXIC ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 8 FDA reports)
NEOPLASM MALIGNANT ( 8 FDA reports)
PSEUDOMONAS INFECTION ( 8 FDA reports)
RENAL FAILURE ACUTE ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
SYNCOPE ( 8 FDA reports)
ANAEMIA ( 7 FDA reports)
ATRIAL FIBRILLATION ( 7 FDA reports)
CARDIOMEGALY ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
COUGH ( 7 FDA reports)
DEEP VEIN THROMBOSIS ( 7 FDA reports)
DRUG INTERACTION ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
CARDIAC ARREST ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CYSTITIS ( 6 FDA reports)
EXTRASYSTOLES ( 6 FDA reports)
FACE OEDEMA ( 6 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
ILEUS PARALYTIC ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
NEOPLASM PROGRESSION ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
STOMATITIS ( 6 FDA reports)
UVEITIS ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
ABNORMAL FAECES ( 5 FDA reports)
ARTHRITIS ( 5 FDA reports)
BURSITIS ( 5 FDA reports)
DRUG HYPERSENSITIVITY ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
ERYSIPELAS ( 5 FDA reports)
FOREARM FRACTURE ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HAND FRACTURE ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
LACERATION ( 5 FDA reports)
LEFT VENTRICULAR FAILURE ( 5 FDA reports)
MUCOSAL INFLAMMATION ( 5 FDA reports)
ORTHOSTATIC HYPOTENSION ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PNEUMOTHORAX ( 5 FDA reports)
PYELONEPHRITIS ACUTE ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
ROTATOR CUFF SYNDROME ( 5 FDA reports)
SKIN DISCOLOURATION ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
TONGUE OEDEMA ( 5 FDA reports)
WOUND INFECTION ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ALVEOLITIS ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
BLOOD ALBUMIN DECREASED ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
CEREBRAL INFARCTION ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CHOLANGITIS ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
COLITIS MICROSCOPIC ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 4 FDA reports)
DIABETES MELLITUS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
HAEMOTHORAX ( 4 FDA reports)
HYPERKINESIA ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PNEUMONITIS ( 4 FDA reports)
POLYNEUROPATHY ( 4 FDA reports)
RENAL CELL CARCINOMA ( 4 FDA reports)
RENAL TUBULAR NECROSIS ( 4 FDA reports)
SHUNT OCCLUSION ( 4 FDA reports)
STREPTOCOCCAL BACTERAEMIA ( 4 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
TRANSPLANT ABSCESS ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 3 FDA reports)
AMPUTATION ( 3 FDA reports)
ANAPHYLACTIC SHOCK ( 3 FDA reports)
APNOEA ( 3 FDA reports)
AREFLEXIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CAROTID ARTERY THROMBOSIS ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEREALISATION ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FRONTOTEMPORAL DEMENTIA ( 3 FDA reports)
GALLBLADDER ENLARGEMENT ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
ILEUS ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LACRIMATION INCREASED ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
NEUROPATHY ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PRIAPISM ( 3 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 3 FDA reports)
PROTEINURIA ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
STOMACH DISCOMFORT ( 3 FDA reports)
STRESS ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
THIRST ( 3 FDA reports)
URINE COLOUR ABNORMAL ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABNORMAL DREAMS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIOPLASTY ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ASCITES ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 2 FDA reports)
AXILLARY PAIN ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BREAST CANCER STAGE II ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARCINOID TUMOUR OF THE DUODENUM ( 2 FDA reports)
CARDIAC ASTHMA ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
COMA ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
CYTOMEGALOVIRUS ANTIBODY POSITIVE ( 2 FDA reports)
DEFICIENCY OF BILE SECRETION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
ECTOPIC PREGNANCY ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING DRUNK ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GASTROINTESTINAL ULCER ( 2 FDA reports)
GOUT ( 2 FDA reports)
GRANULOCYTOPENIA ( 2 FDA reports)
HAEMOLYSIS ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEMIANOPIA ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATIC NECROSIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HEPATITIS A ANTIBODY POSITIVE ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPOKALAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOPHAGIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
IIIRD NERVE DISORDER ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MULTIPLE MYELOMA ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OSTEOSYNTHESIS ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PATELLA FRACTURE ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PLEURAL CALCIFICATION ( 2 FDA reports)
PLEURAL DISORDER ( 2 FDA reports)
PLEURAL EFFUSION ( 2 FDA reports)
POOR QUALITY SLEEP ( 2 FDA reports)
POSTOPERATIVE ADHESION ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PRINZMETAL ANGINA ( 2 FDA reports)
PSORIASIS ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RETINAL VASCULAR THROMBOSIS ( 2 FDA reports)
SECONDARY ADRENOCORTICAL INSUFFICIENCY ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN IRRITATION ( 2 FDA reports)
SMALL INTESTINE CARCINOMA ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STENT OCCLUSION ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TERMINAL STATE ( 2 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TREMOR ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VASCULAR RUPTURE ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEGENER'S GRANULOMATOSIS ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
YAWNING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AMNIORRHOEA ( 1 FDA reports)
AMYLASE INCREASED ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC ANEURYSM ( 1 FDA reports)
AORTIC CALCIFICATION ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTERIAL RESTENOSIS ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUTONOMIC NEUROPATHY ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BILIARY TRACT DISORDER ( 1 FDA reports)
BIOPSY INTESTINE ABNORMAL ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC INFECTION ( 1 FDA reports)
CARDIAC MYXOMA ( 1 FDA reports)
CHILAIDITI'S SYNDROME ( 1 FDA reports)
CHOLAEMIA ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONIC STENOSIS ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CORONARY ANGIOPLASTY ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CORONARY ARTERY SURGERY ( 1 FDA reports)
CROHN'S DISEASE ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DUODENAL OBSTRUCTION ( 1 FDA reports)
DUODENAL STENOSIS ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FACIAL PARESIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FOETAL HYPOKINESIA ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE ABNORMAL ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GENITAL DISORDER MALE ( 1 FDA reports)
GRANULOCYTE COUNT DECREASED ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC INFARCTION ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATIC VEIN OCCLUSION ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HORNER'S SYNDROME ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYDROCHOLECYSTIS ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANT SITE INFECTION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFARCTION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INGUINAL HERNIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
IRIS VASCULAR DISORDER ( 1 FDA reports)
IRITIS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARGE CELL CARCINOMA OF THE RESPIRATORY TRACT STAGE UNSPECIFIED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
METASTASES TO ABDOMINAL CAVITY ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO NECK ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 1 FDA reports)
MYELOFIBROSIS ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROSTOMY TUBE PLACEMENT ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PANCREATIC NECROSIS ( 1 FDA reports)
PAPILLARY TUMOUR OF RENAL PELVIS ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARATHYROID TUMOUR ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PILOERECTION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POSTOPERATIVE ILEUS ( 1 FDA reports)
POVERTY OF SPEECH ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE DELIVERY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESPIRATORY TRACT IRRITATION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETINAL ISCHAEMIA ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN TOXICITY ( 1 FDA reports)
SMALL INTESTINE CARCINOMA METASTATIC ( 1 FDA reports)
SPINAL COLUMN INJURY ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPUTUM INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STRABISMUS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT CANCER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TRANSITIONAL CELL CARCINOMA ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URINARY BLADDER HAEMORRHAGE ( 1 FDA reports)
URINE FLOW DECREASED ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WALKING DISABILITY ( 1 FDA reports)
WHITE BLOOD CELL COUNT ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
XIITH NERVE INJURY ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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