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

HYPOTENSION ( 84 FDA reports)
DYSPNOEA ( 81 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 71 FDA reports)
PNEUMONIA ( 67 FDA reports)
PYREXIA ( 65 FDA reports)
DIARRHOEA ( 54 FDA reports)
NAUSEA ( 50 FDA reports)
PAIN ( 48 FDA reports)
VOMITING ( 43 FDA reports)
CHEST PAIN ( 41 FDA reports)
ANAEMIA ( 39 FDA reports)
ASTHENIA ( 36 FDA reports)
RENAL FAILURE ( 36 FDA reports)
ANXIETY ( 35 FDA reports)
DIZZINESS ( 35 FDA reports)
OEDEMA PERIPHERAL ( 35 FDA reports)
RENAL FAILURE ACUTE ( 35 FDA reports)
HYPOXIA ( 33 FDA reports)
BONE DISORDER ( 32 FDA reports)
RASH ( 32 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 31 FDA reports)
NEUTROPENIA ( 31 FDA reports)
BRONCHITIS ( 27 FDA reports)
FALL ( 27 FDA reports)
FATIGUE ( 27 FDA reports)
PANCYTOPENIA ( 27 FDA reports)
RESPIRATORY FAILURE ( 27 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 27 FDA reports)
COUGH ( 26 FDA reports)
SEPSIS ( 26 FDA reports)
HEADACHE ( 25 FDA reports)
RIB FRACTURE ( 25 FDA reports)
ABDOMINAL PAIN ( 24 FDA reports)
CANDIDIASIS ( 23 FDA reports)
CEREBROVASCULAR ACCIDENT ( 23 FDA reports)
BACK PAIN ( 22 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 22 FDA reports)
SINUSITIS ( 22 FDA reports)
SPINAL COMPRESSION FRACTURE ( 22 FDA reports)
BONE OPERATION ( 21 FDA reports)
DEHYDRATION ( 21 FDA reports)
MULTI-ORGAN FAILURE ( 21 FDA reports)
PLEURAL EFFUSION ( 21 FDA reports)
THROMBOCYTOPENIA ( 21 FDA reports)
ATRIAL FIBRILLATION ( 20 FDA reports)
EMOTIONAL DISTRESS ( 20 FDA reports)
GASTRITIS ( 20 FDA reports)
TREMOR ( 20 FDA reports)
WHEEZING ( 20 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 19 FDA reports)
INFLAMMATION ( 19 FDA reports)
INJURY ( 19 FDA reports)
LYMPHADENOPATHY ( 19 FDA reports)
NEUROPATHY PERIPHERAL ( 19 FDA reports)
ACUTE RESPIRATORY FAILURE ( 18 FDA reports)
BONE PAIN ( 18 FDA reports)
BRADYCARDIA ( 18 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 18 FDA reports)
CATARACT ( 18 FDA reports)
DEATH ( 18 FDA reports)
DRUG INTERACTION ( 18 FDA reports)
OSTEONECROSIS OF JAW ( 18 FDA reports)
PAIN IN EXTREMITY ( 18 FDA reports)
SEPTIC SHOCK ( 18 FDA reports)
CARDIAC ARREST ( 17 FDA reports)
EAR DISCOMFORT ( 17 FDA reports)
FISTULA ( 17 FDA reports)
HAEMATURIA ( 17 FDA reports)
HAEMORRHOIDS ( 17 FDA reports)
HERPES ZOSTER ( 17 FDA reports)
MALAISE ( 17 FDA reports)
MITRAL VALVE INCOMPETENCE ( 17 FDA reports)
SKIN LESION ( 17 FDA reports)
TENDERNESS ( 17 FDA reports)
TOOTH EXTRACTION ( 17 FDA reports)
BLOOD PRESSURE INCREASED ( 16 FDA reports)
BONE MARROW FAILURE ( 16 FDA reports)
CONDITION AGGRAVATED ( 16 FDA reports)
DIVERTICULUM ( 16 FDA reports)
ERECTILE DYSFUNCTION ( 16 FDA reports)
EXOSTOSIS ( 16 FDA reports)
GASTRIC POLYPS ( 16 FDA reports)
GINGIVAL SWELLING ( 16 FDA reports)
HYPERPLASIA ( 16 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 16 FDA reports)
INFECTION ( 16 FDA reports)
LUNG INFILTRATION ( 16 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 16 FDA reports)
OSTEOMYELITIS ( 16 FDA reports)
PNEUMONIA ASPIRATION ( 16 FDA reports)
PRIMARY SEQUESTRUM ( 16 FDA reports)
RESPIRATORY DISTRESS ( 16 FDA reports)
SLEEP APNOEA SYNDROME ( 16 FDA reports)
SOFT TISSUE INFLAMMATION ( 16 FDA reports)
STOMATITIS ( 16 FDA reports)
TOOTH ABSCESS ( 16 FDA reports)
ALVEOLOPLASTY ( 15 FDA reports)
ARTHRALGIA ( 15 FDA reports)
BONE DEBRIDEMENT ( 15 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 15 FDA reports)
DIABETES MELLITUS ( 15 FDA reports)
DRUG INEFFECTIVE ( 15 FDA reports)
EMPHYSEMA ( 15 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 15 FDA reports)
HYPERGLYCAEMIA ( 15 FDA reports)
HYPERHIDROSIS ( 15 FDA reports)
JAW OPERATION ( 15 FDA reports)
MYELOMA RECURRENCE ( 15 FDA reports)
OSTEOARTHRITIS ( 15 FDA reports)
PAIN IN JAW ( 15 FDA reports)
SINUS DISORDER ( 15 FDA reports)
URINARY TRACT INFECTION ( 15 FDA reports)
BONE LESION ( 14 FDA reports)
CATARACT OPERATION ( 14 FDA reports)
CELLULITIS ( 14 FDA reports)
CONSTIPATION ( 14 FDA reports)
DECREASED APPETITE ( 14 FDA reports)
EJECTION FRACTION DECREASED ( 14 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 14 FDA reports)
GINGIVAL DISORDER ( 14 FDA reports)
HYPOAESTHESIA ( 14 FDA reports)
HYPONATRAEMIA ( 14 FDA reports)
INTRAOCULAR LENS IMPLANT ( 14 FDA reports)
LEUKOCYTOSIS ( 14 FDA reports)
LOSS OF CONSCIOUSNESS ( 14 FDA reports)
OXYGEN SUPPLEMENTATION ( 14 FDA reports)
TACHYCARDIA ( 14 FDA reports)
TOOTH IMPACTED ( 14 FDA reports)
BONE MARROW TRANSPLANT ( 13 FDA reports)
CARDIO-RESPIRATORY ARREST ( 13 FDA reports)
CONFUSIONAL STATE ( 13 FDA reports)
FEMUR FRACTURE ( 13 FDA reports)
HYPERLIPIDAEMIA ( 13 FDA reports)
LETHARGY ( 13 FDA reports)
MYOCARDIAL INFARCTION ( 13 FDA reports)
PERICARDIAL EFFUSION ( 13 FDA reports)
PULMONARY EMBOLISM ( 13 FDA reports)
SOMNOLENCE ( 13 FDA reports)
SYNCOPE ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 12 FDA reports)
ASTHMA ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
CARDIAC FAILURE ( 12 FDA reports)
CONTUSION ( 12 FDA reports)
DEFORMITY ( 12 FDA reports)
HAEMATOCRIT DECREASED ( 12 FDA reports)
MENTAL STATUS CHANGES ( 12 FDA reports)
MUSCULOSKELETAL PAIN ( 12 FDA reports)
MYALGIA ( 12 FDA reports)
PHYSICAL DISABILITY ( 12 FDA reports)
SKIN PAPILLOMA ( 12 FDA reports)
UNRESPONSIVE TO STIMULI ( 12 FDA reports)
ABDOMINAL DISTENSION ( 11 FDA reports)
BLOOD GLUCOSE INCREASED ( 11 FDA reports)
CHEST DISCOMFORT ( 11 FDA reports)
CONVULSION ( 11 FDA reports)
HYPERTENSION ( 11 FDA reports)
MACULOPATHY ( 11 FDA reports)
PERIPHERAL ISCHAEMIA ( 11 FDA reports)
PRURITUS ( 11 FDA reports)
PULMONARY OEDEMA ( 11 FDA reports)
AGITATION ( 10 FDA reports)
DEEP VEIN THROMBOSIS ( 10 FDA reports)
DEPRESSION ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
INSOMNIA ( 10 FDA reports)
LIGAMENT RUPTURE ( 10 FDA reports)
METABOLIC ACIDOSIS ( 10 FDA reports)
OXYGEN SATURATION DECREASED ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
SINUS ARRHYTHMIA ( 10 FDA reports)
SPINAL COLUMN STENOSIS ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
ABASIA ( 9 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
BACTERAEMIA ( 9 FDA reports)
CEREBRAL ISCHAEMIA ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 9 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 9 FDA reports)
LIPOATROPHY ( 9 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 9 FDA reports)
LOW TURNOVER OSTEOPATHY ( 9 FDA reports)
MASS ( 9 FDA reports)
METABOLIC ENCEPHALOPATHY ( 9 FDA reports)
MUCOSAL INFLAMMATION ( 9 FDA reports)
NEPHROLITHIASIS ( 9 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 9 FDA reports)
SPINAL FUSION SURGERY ( 9 FDA reports)
SPINAL LAMINECTOMY ( 9 FDA reports)
STRESS FRACTURE ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
TOOTH DISORDER ( 9 FDA reports)
ARTERIOSCLEROSIS ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
CYANOSIS ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
DYSPNOEA EXERTIONAL ( 8 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 8 FDA reports)
LOCALISED INFECTION ( 8 FDA reports)
MEDICATION ERROR ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
PANCREATITIS ACUTE ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
PRODUCTIVE COUGH ( 8 FDA reports)
RENAL FAILURE CHRONIC ( 8 FDA reports)
RHABDOMYOLYSIS ( 8 FDA reports)
SWOLLEN TONGUE ( 8 FDA reports)
VENTRICULAR HYPERTROPHY ( 8 FDA reports)
APHTHOUS STOMATITIS ( 7 FDA reports)
ATELECTASIS ( 7 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
CARDIOGENIC SHOCK ( 7 FDA reports)
CHILLS ( 7 FDA reports)
COMA ( 7 FDA reports)
DECREASED INTEREST ( 7 FDA reports)
DENTAL CARIES ( 7 FDA reports)
DIVERTICULUM INTESTINAL ( 7 FDA reports)
DRUG HYPERSENSITIVITY ( 7 FDA reports)
DYSKINESIA ( 7 FDA reports)
DYSPHEMIA ( 7 FDA reports)
EOSINOPHIL COUNT INCREASED ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
FEBRILE NEUTROPENIA ( 7 FDA reports)
FLUID OVERLOAD ( 7 FDA reports)
GINGIVITIS ( 7 FDA reports)
HAEMORRHAGE ( 7 FDA reports)
INJECTION SITE HAEMATOMA ( 7 FDA reports)
METASTASES TO BONE ( 7 FDA reports)
NEURODERMATITIS ( 7 FDA reports)
ONYCHOMYCOSIS ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
OSTEOPENIA ( 7 FDA reports)
OSTEOPOROSIS ( 7 FDA reports)
OSTEOSCLEROSIS ( 7 FDA reports)
OTITIS MEDIA ( 7 FDA reports)
PNEUMONIA VIRAL ( 7 FDA reports)
PROSTATE CANCER ( 7 FDA reports)
PROSTATOMEGALY ( 7 FDA reports)
RALES ( 7 FDA reports)
RENAL CYST ( 7 FDA reports)
TENDONITIS ( 7 FDA reports)
TREATMENT NONCOMPLIANCE ( 7 FDA reports)
TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
DEBRIDEMENT ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
ECCHYMOSIS ( 6 FDA reports)
ENCEPHALOPATHY ( 6 FDA reports)
FUNGAL INFECTION ( 6 FDA reports)
JOINT ARTHROPLASTY ( 6 FDA reports)
MUSCLE HAEMORRHAGE ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
PARAPARESIS ( 6 FDA reports)
PERIPHERAL EMBOLISM ( 6 FDA reports)
PERITONITIS ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PULMONARY HYPERTENSION ( 6 FDA reports)
SKIN DISCOLOURATION ( 6 FDA reports)
TENDON GRAFT ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
VASCULAR INSUFFICIENCY ( 6 FDA reports)
VENTRICULAR TACHYCARDIA ( 6 FDA reports)
VIRAL INFECTION ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ACIDOSIS ( 5 FDA reports)
ADVERSE DRUG REACTION ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
APHASIA ( 5 FDA reports)
CARDIAC DISORDER ( 5 FDA reports)
DEVICE RELATED SEPSIS ( 5 FDA reports)
DYSARTHRIA ( 5 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 5 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GASTRIC ULCER ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPERKALAEMIA ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
HYPOVOLAEMIA ( 5 FDA reports)
INCREASED TENDENCY TO BRUISE ( 5 FDA reports)
LEUKOPENIA ( 5 FDA reports)
OEDEMA ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
PEPTIC ULCER ( 5 FDA reports)
PNEUMONITIS ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
SERUM FERRITIN INCREASED ( 5 FDA reports)
SPINAL DISORDER ( 5 FDA reports)
SPINAL OSTEOARTHRITIS ( 5 FDA reports)
STEM CELL TRANSPLANT ( 5 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 5 FDA reports)
THROMBOSIS ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
AMNESIA ( 4 FDA reports)
AORTIC ANEURYSM ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ATRIAL NATRIURETIC PEPTIDE INCREASED ( 4 FDA reports)
BLISTER ( 4 FDA reports)
BLOOD CALCIUM INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 4 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 4 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 4 FDA reports)
BONE SCAN ABNORMAL ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
DENERVATION ATROPHY ( 4 FDA reports)
DEVICE MALFUNCTION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG DOSE OMISSION ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
FAECAL INCONTINENCE ( 4 FDA reports)
FEAR ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
HAEMATOMA ( 4 FDA reports)
HAEMODIALYSIS ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYPERNATRAEMIA ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 4 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LUNG INFECTION ( 4 FDA reports)
LYMPHOPENIA ( 4 FDA reports)
MENTAL DISORDER DUE TO A GENERAL MEDICAL CONDITION ( 4 FDA reports)
MENTAL IMPAIRMENT ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
MYOPATHY ( 4 FDA reports)
NORMAL NEWBORN ( 4 FDA reports)
OEDEMA MOUTH ( 4 FDA reports)
ORAL CANDIDIASIS ( 4 FDA reports)
PANCREATIC DISORDER ( 4 FDA reports)
PERIODONTAL DISEASE ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
POISONING ( 4 FDA reports)
POSTOPERATIVE ILEUS ( 4 FDA reports)
PROCEDURAL COMPLICATION ( 4 FDA reports)
PSYCHOTIC DISORDER ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
RADICULOPATHY ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
TOOTH FRACTURE ( 4 FDA reports)
TOOTH LOSS ( 4 FDA reports)
TROPONIN INCREASED ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
ABDOMINAL PAIN LOWER ( 3 FDA reports)
ABSCESS LIMB ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ADVERSE EVENT ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ALLERGIC GRANULOMATOUS ANGIITIS ( 3 FDA reports)
ANION GAP INCREASED ( 3 FDA reports)
ASCITES ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
AUTOLOGOUS BONE MARROW TRANSPLANTATION THERAPY ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BACTERIAL INFECTION ( 3 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 3 FDA reports)
BLADDER PERFORATION ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CARDIAC TAMPONADE ( 3 FDA reports)
CEREBRAL ATROPHY ( 3 FDA reports)
COLON ADENOMA ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DRUG EFFECT DECREASED ( 3 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 3 FDA reports)
DRUG TOXICITY ( 3 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EXTREMITY NECROSIS ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATIC ENCEPHALOPATHY ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HEPATITIS ( 3 FDA reports)
HYPEROSMOLAR STATE ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
IRON OVERLOAD ( 3 FDA reports)
LABORATORY TEST ABNORMAL ( 3 FDA reports)
LACTIC ACIDOSIS ( 3 FDA reports)
LOBAR PNEUMONIA ( 3 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 3 FDA reports)
MALNUTRITION ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MESOTHELIOMA ( 3 FDA reports)
METABOLIC SYNDROME ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NEPHRITIC SYNDROME ( 3 FDA reports)
NEURALGIA ( 3 FDA reports)
NIGHT SWEATS ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
PAIN OF SKIN ( 3 FDA reports)
PALLOR ( 3 FDA reports)
PERICARDIAL DRAINAGE ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 3 FDA reports)
PULMONARY HILUM MASS ( 3 FDA reports)
RASH ERYTHEMATOUS ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESPIRATORY SYNCYTIAL VIRUS INFECTION ( 3 FDA reports)
RESPIRATORY TRACT INFLAMMATION ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
STREPTOCOCCAL SEPSIS ( 3 FDA reports)
STRESS ( 3 FDA reports)
STRESS URINARY INCONTINENCE ( 3 FDA reports)
SUBSTANCE ABUSE ( 3 FDA reports)
TACHYCARDIA PAROXYSMAL ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
UNDERDOSE ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ACTINOMYCES TEST POSITIVE ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
AORTIC STENOSIS ( 2 FDA reports)
APNOEA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
AZOTAEMIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BIPOLAR DISORDER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE ORTHOSTATIC DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BRONCHIAL HYPERREACTIVITY ( 2 FDA reports)
CALCIPHYLAXIS ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE SEPSIS ( 2 FDA reports)
COLECTOMY ( 2 FDA reports)
CONTRAST MEDIA REACTION ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIABETIC NEPHROPATHY ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DRUG LEVEL DECREASED ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 2 FDA reports)
ENDOTRACHEAL INTUBATION ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
EXCORIATION ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
GASTRITIS EROSIVE ( 2 FDA reports)
GASTROINTESTINAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 2 FDA reports)
GINGIVAL ULCERATION ( 2 FDA reports)
GOITRE ( 2 FDA reports)
HAEMOCHROMATOSIS ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEREDITARY DISORDER ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPOAESTHESIA FACIAL ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
ILL-DEFINED DISORDER ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 2 FDA reports)
KETONURIA ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LABORATORY TEST INTERFERENCE ( 2 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MANIA ( 2 FDA reports)
MEAN CELL HAEMOGLOBIN INCREASED ( 2 FDA reports)
MEAN CELL VOLUME INCREASED ( 2 FDA reports)
MECHANICAL VENTILATION ( 2 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 2 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 2 FDA reports)
MONOCYTE COUNT INCREASED ( 2 FDA reports)
MOVEMENT DISORDER ( 2 FDA reports)
MUSCLE TIGHTNESS ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROPATHY TOXIC ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OCCULT BLOOD POSITIVE ( 2 FDA reports)
OESOPHAGEAL STENOSIS ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARTIAL SEIZURES WITH SECONDARY GENERALISATION ( 2 FDA reports)
PERITONEAL DISORDER ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
POST PROCEDURAL HAEMATOMA ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PSEUDOMONAL BACTERAEMIA ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 2 FDA reports)
SNORING ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
VASCULAR DEMENTIA ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VENTRICULAR HYPOKINESIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACQUIRED IMMUNODEFICIENCY SYNDROME ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ACUTE PROMYELOCYTIC LEUKAEMIA ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALLERGY TO CHEMICALS ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANION GAP DECREASED ( 1 FDA reports)
ANTIBIOTIC THERAPY ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE DECREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BASOPHIL COUNT INCREASED ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD PRODUCT TRANSFUSION DEPENDENT ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN INJURY ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN SCAN ABNORMAL ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHIAL HAEMORRHAGE ( 1 FDA reports)
BRONCHITIS CHRONIC ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
BRONCHOSCOPY ABNORMAL ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CAUTERY TO NOSE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL MICROANGIOPATHY ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHROMATOPSIA ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC RESPIRATORY FAILURE ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLONOSCOPY ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 1 FDA reports)
CORONARY ARTERY BYPASS ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
DEATH OF RELATIVE ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DELAYED RECOVERY FROM ANAESTHESIA ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG CLEARANCE DECREASED ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSPNOEA PAROXYSMAL NOCTURNAL ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
ENDOCARDITIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
EROSIVE OESOPHAGITIS ( 1 FDA reports)
ESCHERICHIA BACTERAEMIA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EX-TOBACCO USER ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EXTUBATION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FLAT AFFECT ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
GALLOP RHYTHM PRESENT ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL TUBE INSERTION ( 1 FDA reports)
GASTROSTOMY TUBE INSERTION ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HALLUCINATION, AUDITORY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HELICOBACTER GASTRITIS ( 1 FDA reports)
HELICOBACTER TEST POSITIVE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATIC PAIN ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPERVOLAEMIA ( 1 FDA reports)
HYPOPERFUSION ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFUSION SITE DISCOLOURATION ( 1 FDA reports)
INHALATION THERAPY ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INTERMITTENT CLAUDICATION ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTESTINAL DILATATION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
ISCHAEMIC NEPHROPATHY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKAEMIA PLASMACYTIC ( 1 FDA reports)
LEUKAEMIA RECURRENT ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LYMPHOCYTE COUNT INCREASED ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEAN CELL VOLUME ABNORMAL ( 1 FDA reports)
MEASLES ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MINERAL DEFICIENCY ( 1 FDA reports)
MONOCYTE PERCENTAGE INCREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
MYOCLONIC EPILEPSY ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OBSESSIVE THOUGHTS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OESOPHAGOGASTRODUODENOSCOPY ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL MUCOSAL BLISTERING ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEORADIONECROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC CARCINOMA METASTATIC ( 1 FDA reports)
PANCREATITIS NECROTISING ( 1 FDA reports)
PANCREATITIS RELAPSING ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHOTODYNAMIC THERAPY ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI INFECTION ( 1 FDA reports)
PNEUMONIA HAEMOPHILUS ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POST-TRAUMATIC PAIN ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL HYPOTENSION ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PYROGLUTAMATE INCREASED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RAYNAUD'S PHENOMENON ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEASONAL AFFECTIVE DISORDER ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN TURGOR DECREASED ( 1 FDA reports)
SLEEP ATTACKS ( 1 FDA reports)
SLOW RESPONSE TO STIMULI ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STARVATION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUPPLEMENTATION THERAPY ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TERMINAL STATE ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TYPE 1 DIABETES MELLITUS ( 1 FDA reports)
UHTHOFF'S PHENOMENON ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULITIC RASH ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASOPRESSIVE THERAPY ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WEANING FAILURE ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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