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

DEATH ( 412 FDA reports)
CHEST PAIN ( 261 FDA reports)
PAIN ( 154 FDA reports)
HYPOTENSION ( 135 FDA reports)
NAUSEA ( 134 FDA reports)
CEREBRAL HAEMORRHAGE ( 131 FDA reports)
VOMITING ( 112 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 100 FDA reports)
DYSPNOEA ( 95 FDA reports)
DRUG INEFFECTIVE ( 90 FDA reports)
VENTRICULAR TACHYCARDIA ( 84 FDA reports)
ANXIETY ( 83 FDA reports)
HAEMORRHAGE ( 77 FDA reports)
RESPIRATORY FAILURE ( 76 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 75 FDA reports)
PNEUMONIA ( 72 FDA reports)
BRADYCARDIA ( 69 FDA reports)
HYPERTENSION ( 67 FDA reports)
OEDEMA PERIPHERAL ( 62 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 58 FDA reports)
DEEP VEIN THROMBOSIS ( 57 FDA reports)
CHEST DISCOMFORT ( 56 FDA reports)
PYREXIA ( 55 FDA reports)
PULMONARY EMBOLISM ( 54 FDA reports)
DIARRHOEA ( 49 FDA reports)
ANGIOEDEMA ( 47 FDA reports)
BACK PAIN ( 44 FDA reports)
VENTRICULAR FIBRILLATION ( 44 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 42 FDA reports)
INJURY ( 40 FDA reports)
MULTI-ORGAN FAILURE ( 40 FDA reports)
RENAL FAILURE ACUTE ( 40 FDA reports)
CARDIAC ARREST ( 39 FDA reports)
CEREBROVASCULAR ACCIDENT ( 39 FDA reports)
HEADACHE ( 39 FDA reports)
NEUROPATHY PERIPHERAL ( 39 FDA reports)
OSTEONECROSIS OF JAW ( 39 FDA reports)
BLOOD PRESSURE DECREASED ( 38 FDA reports)
CEREBRAL INFARCTION ( 38 FDA reports)
COUGH ( 38 FDA reports)
THROMBOCYTOPENIA ( 38 FDA reports)
ABDOMINAL PAIN ( 37 FDA reports)
GAIT DISTURBANCE ( 37 FDA reports)
HYPERHIDROSIS ( 37 FDA reports)
TACHYCARDIA ( 37 FDA reports)
BRAIN OEDEMA ( 36 FDA reports)
MYOCARDIAL INFARCTION ( 36 FDA reports)
SINUS BRADYCARDIA ( 36 FDA reports)
PNEUMOTHORAX ( 34 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 33 FDA reports)
INSOMNIA ( 33 FDA reports)
PAIN IN EXTREMITY ( 33 FDA reports)
ARRHYTHMIA ( 32 FDA reports)
ATRIAL FIBRILLATION ( 32 FDA reports)
CARDIOMEGALY ( 32 FDA reports)
CONVULSION ( 32 FDA reports)
ANHEDONIA ( 31 FDA reports)
ATELECTASIS ( 31 FDA reports)
DIZZINESS ( 31 FDA reports)
RASH ( 30 FDA reports)
SPINAL OSTEOARTHRITIS ( 30 FDA reports)
DRUG INTERACTION ( 29 FDA reports)
MASTICATION DISORDER ( 29 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 28 FDA reports)
HYPOAESTHESIA ( 28 FDA reports)
OSTEOPENIA ( 28 FDA reports)
SOMNOLENCE ( 28 FDA reports)
ASTHENIA ( 27 FDA reports)
CARDIOGENIC SHOCK ( 27 FDA reports)
ISCHAEMIC STROKE ( 27 FDA reports)
DISCOMFORT ( 26 FDA reports)
LOSS OF CONSCIOUSNESS ( 26 FDA reports)
PULMONARY HAEMORRHAGE ( 26 FDA reports)
PULMONARY OEDEMA ( 26 FDA reports)
ANAEMIA ( 25 FDA reports)
BONE DISORDER ( 25 FDA reports)
DYSPHAGIA ( 25 FDA reports)
FALL ( 25 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 25 FDA reports)
MENTAL STATUS CHANGES ( 25 FDA reports)
PLEURAL EFFUSION ( 25 FDA reports)
DEPRESSION ( 24 FDA reports)
OSTEOPOROSIS ( 24 FDA reports)
RENAL FAILURE ( 24 FDA reports)
CARDIO-RESPIRATORY ARREST ( 23 FDA reports)
EMOTIONAL DISTRESS ( 23 FDA reports)
HAEMATOMA ( 23 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 23 FDA reports)
PULMONARY FIBROSIS ( 23 FDA reports)
SEPSIS ( 23 FDA reports)
SINUS TACHYCARDIA ( 23 FDA reports)
VISION BLURRED ( 23 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 22 FDA reports)
ARTHRALGIA ( 22 FDA reports)
CARDIAC FAILURE ( 22 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 22 FDA reports)
CYANOSIS ( 22 FDA reports)
OSTEOARTHRITIS ( 22 FDA reports)
PULMONARY HYPERTENSION ( 22 FDA reports)
VENA CAVA THROMBOSIS ( 22 FDA reports)
GASTRITIS ( 21 FDA reports)
HAEMOGLOBIN DECREASED ( 21 FDA reports)
MUSCULOSKELETAL PAIN ( 21 FDA reports)
PAIN IN JAW ( 21 FDA reports)
PARAESTHESIA ( 21 FDA reports)
WEIGHT DECREASED ( 21 FDA reports)
COMA ( 20 FDA reports)
CONFUSIONAL STATE ( 20 FDA reports)
DEFORMITY ( 20 FDA reports)
EPISTAXIS ( 20 FDA reports)
EXTRASYSTOLES ( 20 FDA reports)
FAECAL INCONTINENCE ( 20 FDA reports)
SINUSITIS ( 20 FDA reports)
TOOTH FRACTURE ( 20 FDA reports)
UNRESPONSIVE TO STIMULI ( 20 FDA reports)
URINARY INCONTINENCE ( 20 FDA reports)
HAEMORRHAGIC TRANSFORMATION STROKE ( 19 FDA reports)
HEMIPARESIS ( 19 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 19 FDA reports)
LIFE EXPECTANCY SHORTENED ( 19 FDA reports)
PNEUMONIA ASPIRATION ( 19 FDA reports)
TOOTH DISORDER ( 19 FDA reports)
ABSCESS ( 18 FDA reports)
ANAPHYLACTIC REACTION ( 18 FDA reports)
CNS VENTRICULITIS ( 18 FDA reports)
EMPHYSEMA ( 18 FDA reports)
EPILEPSY ( 18 FDA reports)
HYPOXIA ( 18 FDA reports)
ROTATOR CUFF SYNDROME ( 18 FDA reports)
SCAR ( 18 FDA reports)
SHOCK ( 18 FDA reports)
AGITATION ( 17 FDA reports)
ANAPHYLACTIC SHOCK ( 17 FDA reports)
BLOOD PRESSURE INCREASED ( 17 FDA reports)
EMPYEMA ( 17 FDA reports)
FAILURE TO THRIVE ( 17 FDA reports)
FATIGUE ( 17 FDA reports)
KLEBSIELLA SEPSIS ( 17 FDA reports)
MUSCULAR WEAKNESS ( 17 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 17 FDA reports)
NEUTROPENIA ( 17 FDA reports)
OEDEMA ( 17 FDA reports)
RENAL VEIN THROMBOSIS ( 17 FDA reports)
URINARY TRACT INFECTION ( 17 FDA reports)
CERVICAL SPINAL STENOSIS ( 16 FDA reports)
FOOT FRACTURE ( 16 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 16 FDA reports)
INTRACARDIAC THROMBUS ( 16 FDA reports)
LUNG DISORDER ( 16 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 16 FDA reports)
OVERDOSE ( 16 FDA reports)
PRIMARY SEQUESTRUM ( 16 FDA reports)
RETCHING ( 16 FDA reports)
RHINITIS ( 16 FDA reports)
RIB FRACTURE ( 16 FDA reports)
SKIN TIGHTNESS ( 16 FDA reports)
SWOLLEN TONGUE ( 16 FDA reports)
BRAIN HERNIATION ( 15 FDA reports)
CEREBROVASCULAR DISORDER ( 15 FDA reports)
DECREASED INTEREST ( 15 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 15 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 15 FDA reports)
DYSPNOEA EXERTIONAL ( 15 FDA reports)
HYPOPHAGIA ( 15 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 15 FDA reports)
JOINT CONTRACTURE ( 15 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 15 FDA reports)
LEUKOCYTOSIS ( 15 FDA reports)
LUNG INFECTION ( 15 FDA reports)
REPERFUSION ARRHYTHMIA ( 15 FDA reports)
RESPIRATORY ARREST ( 15 FDA reports)
TIBIA FRACTURE ( 15 FDA reports)
TOOTHACHE ( 15 FDA reports)
WHEEZING ( 15 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 15 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 14 FDA reports)
BACTERIAL DISEASE CARRIER ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 14 FDA reports)
BRONCHOPLEURAL FISTULA ( 14 FDA reports)
CHONDROMALACIA ( 14 FDA reports)
CYST ( 14 FDA reports)
DEHYDRATION ( 14 FDA reports)
DIVERTICULUM INTESTINAL ( 14 FDA reports)
ERYTHEMA ( 14 FDA reports)
EYE DISCHARGE ( 14 FDA reports)
FIBULA FRACTURE ( 14 FDA reports)
FOOT DEFORMITY ( 14 FDA reports)
HAEMOPTYSIS ( 14 FDA reports)
HYDROPNEUMOTHORAX ( 14 FDA reports)
INJURY CORNEAL ( 14 FDA reports)
LIP AND/OR ORAL CAVITY CANCER ( 14 FDA reports)
LIP DISCOLOURATION ( 14 FDA reports)
LUNG NEOPLASM MALIGNANT ( 14 FDA reports)
MENOPAUSE ( 14 FDA reports)
OSTEOMYELITIS ( 14 FDA reports)
OSTEORADIONECROSIS ( 14 FDA reports)
PLATELET COUNT DECREASED ( 14 FDA reports)
PULMONARY AIR LEAKAGE ( 14 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 14 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 14 FDA reports)
ANGINA PECTORIS ( 13 FDA reports)
ASPIRATION ( 13 FDA reports)
BLOOD CALCIUM DECREASED ( 13 FDA reports)
BLOOD UREA NITROGEN/CREATININE RATIO INCREASED ( 13 FDA reports)
CARDIAC TAMPONADE ( 13 FDA reports)
HAEMATOCRIT DECREASED ( 13 FDA reports)
HYPERSENSITIVITY ( 13 FDA reports)
HYPOKALAEMIA ( 13 FDA reports)
IMPAIRED HEALING ( 13 FDA reports)
LACERATION ( 13 FDA reports)
LETHARGY ( 13 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 13 FDA reports)
METABOLIC ACIDOSIS ( 13 FDA reports)
MYOCARDIAL RUPTURE ( 13 FDA reports)
NECK PAIN ( 13 FDA reports)
NO THERAPEUTIC RESPONSE ( 13 FDA reports)
PLEURITIC PAIN ( 13 FDA reports)
SKIN LESION ( 13 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 13 FDA reports)
TREMOR ( 13 FDA reports)
ABDOMINAL PAIN UPPER ( 12 FDA reports)
APHASIA ( 12 FDA reports)
ATRIAL FLUTTER ( 12 FDA reports)
COLONIC POLYP ( 12 FDA reports)
COMPARTMENT SYNDROME ( 12 FDA reports)
DISEASE RECURRENCE ( 12 FDA reports)
DYSPEPSIA ( 12 FDA reports)
METASTASES TO LYMPH NODES ( 12 FDA reports)
SEPTIC SHOCK ( 12 FDA reports)
SKIN DISCOLOURATION ( 12 FDA reports)
SWELLING ( 12 FDA reports)
TENDON RUPTURE ( 12 FDA reports)
TOOTH EXTRACTION ( 12 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 12 FDA reports)
TUMOUR LYSIS SYNDROME ( 12 FDA reports)
ASTHMA ( 11 FDA reports)
CANDIDIASIS ( 11 FDA reports)
CELLULITIS ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
EAR PAIN ( 11 FDA reports)
MUCOSAL INFLAMMATION ( 11 FDA reports)
MUSCLE SPASMS ( 11 FDA reports)
PERITONITIS BACTERIAL ( 11 FDA reports)
RECTAL POLYP ( 11 FDA reports)
SKIN DISORDER ( 11 FDA reports)
SKIN HYPERPIGMENTATION ( 11 FDA reports)
SKIN HYPERTROPHY ( 11 FDA reports)
SKIN INDURATION ( 11 FDA reports)
STAPHYLOCOCCAL INFECTION ( 11 FDA reports)
STEM CELL TRANSPLANT ( 11 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 11 FDA reports)
TOOTH LOSS ( 11 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 11 FDA reports)
ABDOMINAL DISTENSION ( 10 FDA reports)
ALOPECIA ( 10 FDA reports)
AORTIC ANEURYSM RUPTURE ( 10 FDA reports)
ARTHRITIS ( 10 FDA reports)
ASCITES ( 10 FDA reports)
BASAL CELL CARCINOMA ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
BONE LESION ( 10 FDA reports)
BREAST CALCIFICATIONS ( 10 FDA reports)
FEBRILE NEUTROPENIA ( 10 FDA reports)
GLAUCOMA ( 10 FDA reports)
HEART RATE INCREASED ( 10 FDA reports)
HYPONATRAEMIA ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
MEDICATION ERROR ( 10 FDA reports)
METASTASES TO LIVER ( 10 FDA reports)
MOBILITY DECREASED ( 10 FDA reports)
NEOPLASM MALIGNANT ( 10 FDA reports)
PALLOR ( 10 FDA reports)
PERIPHERAL ISCHAEMIA ( 10 FDA reports)
PLEURAL FIBROSIS ( 10 FDA reports)
RESTLESSNESS ( 10 FDA reports)
RHYTHM IDIOVENTRICULAR ( 10 FDA reports)
VITREOUS HAEMORRHAGE ( 10 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 10 FDA reports)
ABASIA ( 9 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST ( 9 FDA reports)
AORTIC DISSECTION ( 9 FDA reports)
ARTERIOSCLEROSIS ( 9 FDA reports)
BACTERAEMIA ( 9 FDA reports)
BLOOD POTASSIUM DECREASED ( 9 FDA reports)
BREAST CANCER METASTATIC ( 9 FDA reports)
BRONCHITIS ( 9 FDA reports)
CATHETER PLACEMENT ( 9 FDA reports)
CEREBRAL HAEMATOMA ( 9 FDA reports)
CHILLS ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
DERMATITIS BULLOUS ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
ENCEPHALOPATHY ( 9 FDA reports)
FISTULA ( 9 FDA reports)
GINGIVAL BLEEDING ( 9 FDA reports)
HAEMORRHAGIC STROKE ( 9 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
HYPOVOLAEMIA ( 9 FDA reports)
INFUSION RELATED REACTION ( 9 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 9 FDA reports)
IRRITABLE BOWEL SYNDROME ( 9 FDA reports)
MALNUTRITION ( 9 FDA reports)
METASTASES TO BONE ( 9 FDA reports)
METASTASES TO LUNG ( 9 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 9 FDA reports)
OROPHARYNGEAL PAIN ( 9 FDA reports)
OXYGEN SATURATION DECREASED ( 9 FDA reports)
PATHOLOGICAL FRACTURE ( 9 FDA reports)
PHYSICAL DISABILITY ( 9 FDA reports)
PULSE ABSENT ( 9 FDA reports)
RENAL INFARCT ( 9 FDA reports)
SINUS CONGESTION ( 9 FDA reports)
SKIN NEOPLASM EXCISION ( 9 FDA reports)
SWELLING FACE ( 9 FDA reports)
THROMBOSIS ( 9 FDA reports)
VENTRICULAR HYPOKINESIA ( 9 FDA reports)
AGGRESSION ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 8 FDA reports)
BONE DEBRIDEMENT ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 8 FDA reports)
DYSARTHRIA ( 8 FDA reports)
EMBOLISM ( 8 FDA reports)
FIBRIN D DIMER INCREASED ( 8 FDA reports)
FLUID OVERLOAD ( 8 FDA reports)
FLUSHING ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
HAEMATEMESIS ( 8 FDA reports)
HAEMODYNAMIC INSTABILITY ( 8 FDA reports)
HEMIANOPIA ( 8 FDA reports)
HYDROCEPHALUS ( 8 FDA reports)
INCISION SITE INFECTION ( 8 FDA reports)
JAW FRACTURE ( 8 FDA reports)
JOINT STIFFNESS ( 8 FDA reports)
LOOSE TOOTH ( 8 FDA reports)
PARAESTHESIA ORAL ( 8 FDA reports)
PERICARDIAL EFFUSION ( 8 FDA reports)
PULMONARY CONGESTION ( 8 FDA reports)
PULSELESS ELECTRICAL ACTIVITY ( 8 FDA reports)
RESPIRATORY DISTRESS ( 8 FDA reports)
TACHYPNOEA ( 8 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 8 FDA reports)
TONGUE OEDEMA ( 8 FDA reports)
VENTRICULAR ARRHYTHMIA ( 8 FDA reports)
VISUAL ACUITY REDUCED ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
ARTERY DISSECTION ( 7 FDA reports)
ARTHROSCOPIC SURGERY ( 7 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 7 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 7 FDA reports)
BRADYARRHYTHMIA ( 7 FDA reports)
BRAIN DEATH ( 7 FDA reports)
COSTOCHONDRITIS ( 7 FDA reports)
DRY SKIN ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
ECCHYMOSIS ( 7 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 7 FDA reports)
HEPATIC FAILURE ( 7 FDA reports)
HIATUS HERNIA ( 7 FDA reports)
INTERCOSTAL NEURALGIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 7 FDA reports)
IRRITABILITY ( 7 FDA reports)
MYOCARDIAL FIBROSIS ( 7 FDA reports)
NODAL RHYTHM ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PRURITUS ( 7 FDA reports)
PRURITUS GENERALISED ( 7 FDA reports)
RENAL DISORDER ( 7 FDA reports)
RENAL FAILURE CHRONIC ( 7 FDA reports)
URINARY RETENTION ( 7 FDA reports)
ACIDOSIS ( 6 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 6 FDA reports)
ALLODYNIA ( 6 FDA reports)
AORTIC THROMBOSIS ( 6 FDA reports)
APNOEA ( 6 FDA reports)
BALANCE DISORDER ( 6 FDA reports)
BLINDNESS ( 6 FDA reports)
BLOOD UREA INCREASED ( 6 FDA reports)
BONE EROSION ( 6 FDA reports)
BRAIN STEM HAEMORRHAGE ( 6 FDA reports)
BREAST CANCER RECURRENT ( 6 FDA reports)
CANCER PAIN ( 6 FDA reports)
CATARACT ( 6 FDA reports)
CHOLELITHIASIS ( 6 FDA reports)
CHRONIC SINUSITIS ( 6 FDA reports)
COAGULOPATHY ( 6 FDA reports)
CORNEAL EROSION ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DILATATION VENTRICULAR ( 6 FDA reports)
ENDOCARDITIS ( 6 FDA reports)
FEELING HOT ( 6 FDA reports)
GINGIVITIS ( 6 FDA reports)
GRAND MAL CONVULSION ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HAEMOTHORAX ( 6 FDA reports)
HEMIPLEGIA ( 6 FDA reports)
HERPES ZOSTER ( 6 FDA reports)
HOT FLUSH ( 6 FDA reports)
HYPERAESTHESIA ( 6 FDA reports)
INFARCTION ( 6 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
LUNG INFILTRATION ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
MACULAR OEDEMA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
MENTAL DISORDER ( 6 FDA reports)
MUSCLE TIGHTNESS ( 6 FDA reports)
MYOCARDIAL ISCHAEMIA ( 6 FDA reports)
NASAL CONGESTION ( 6 FDA reports)
NEURITIS ( 6 FDA reports)
NEUROLOGICAL DECOMPENSATION ( 6 FDA reports)
OLIGURIA ( 6 FDA reports)
ORAL PAIN ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
PHAEOCHROMOCYTOMA ( 6 FDA reports)
PROCEDURAL COMPLICATION ( 6 FDA reports)
RALES ( 6 FDA reports)
RASH PAPULAR ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
RENAL TUBULAR NECROSIS ( 6 FDA reports)
SERUM FERRITIN INCREASED ( 6 FDA reports)
SKIN FIBROSIS ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
STATUS EPILEPTICUS ( 6 FDA reports)
TENDERNESS ( 6 FDA reports)
THROAT IRRITATION ( 6 FDA reports)
WRONG DRUG ADMINISTERED ( 6 FDA reports)
ACUTE SINUSITIS ( 5 FDA reports)
AMPUTATION ( 5 FDA reports)
AORTIC ANEURYSM ( 5 FDA reports)
APATHY ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 5 FDA reports)
BACTERIAL INFECTION ( 5 FDA reports)
BLISTER ( 5 FDA reports)
BLOOD ALBUMIN DECREASED ( 5 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 5 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 5 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 5 FDA reports)
BONE MARROW FAILURE ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CATARACT OPERATION ( 5 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 5 FDA reports)
CEREBRAL ARTERY EMBOLISM ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
CHEST TUBE INSERTION ( 5 FDA reports)
COMPRESSION FRACTURE ( 5 FDA reports)
CYSTITIS ( 5 FDA reports)
DEBRIDEMENT ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
DEVICE RELATED INFECTION ( 5 FDA reports)
DRUG ADMINISTRATION ERROR ( 5 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
DRUG INTOLERANCE ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
EJECTION FRACTION DECREASED ( 5 FDA reports)
EMPYEMA DRAINAGE ( 5 FDA reports)
ENDODONTIC PROCEDURE ( 5 FDA reports)
ENDOTRACHEAL INTUBATION ( 5 FDA reports)
EXTREMITY CONTRACTURE ( 5 FDA reports)
FIBROSIS ( 5 FDA reports)
FISTULA DISCHARGE ( 5 FDA reports)
GASTRIC HAEMORRHAGE ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HIP FRACTURE ( 5 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 5 FDA reports)
LUNG OPERATION ( 5 FDA reports)
MACULAR HOLE ( 5 FDA reports)
MAMMOPLASTY ( 5 FDA reports)
MELANOCYTIC NAEVUS ( 5 FDA reports)
METASTASES TO MOUTH ( 5 FDA reports)
METASTATIC NEOPLASM ( 5 FDA reports)
MUSCLE DISORDER ( 5 FDA reports)
MUSCLE FLAP OPERATION ( 5 FDA reports)
NEOPLASM PROGRESSION ( 5 FDA reports)
NEUROLOGICAL SYMPTOM ( 5 FDA reports)
NUTRITIONAL CONDITION ABNORMAL ( 5 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 5 FDA reports)
ODYNOPHAGIA ( 5 FDA reports)
OSTEONECROSIS ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PERICARDIAL HAEMORRHAGE ( 5 FDA reports)
PROTHROMBIN TIME PROLONGED ( 5 FDA reports)
PUNCTURE SITE HAEMORRHAGE ( 5 FDA reports)
RECTAL HAEMORRHAGE ( 5 FDA reports)
REPERFUSION INJURY ( 5 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 5 FDA reports)
ROTATOR CUFF REPAIR ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
SHOCK HAEMORRHAGIC ( 5 FDA reports)
SINUS DISORDER ( 5 FDA reports)
SINUS OPERATION ( 5 FDA reports)
SKIN EXFOLIATION ( 5 FDA reports)
SKIN PLAQUE ( 5 FDA reports)
SKIN WRINKLING ( 5 FDA reports)
TENDON PAIN ( 5 FDA reports)
THORACOTOMY ( 5 FDA reports)
TRACHEAL OEDEMA ( 5 FDA reports)
TRACHEAL STENOSIS ( 5 FDA reports)
UNEVALUABLE EVENT ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
UTERINE PROLAPSE ( 5 FDA reports)
VASCULAR PSEUDOANEURYSM ( 5 FDA reports)
WHEELCHAIR USER ( 5 FDA reports)
WOUND DEHISCENCE ( 5 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 4 FDA reports)
ABSCESS JAW ( 4 FDA reports)
ACTINOMYCOSIS ( 4 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
AGRANULOCYTOSIS ( 4 FDA reports)
ANGIONEUROTIC OEDEMA ( 4 FDA reports)
ANGIOPATHY ( 4 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 4 FDA reports)
AREFLEXIA ( 4 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASPIRATION PLEURAL CAVITY ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
BLINDNESS UNILATERAL ( 4 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 4 FDA reports)
BRAIN MIDLINE SHIFT ( 4 FDA reports)
BREAST PAIN ( 4 FDA reports)
CARDIAC DEATH ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CAROTID ARTERY OCCLUSION ( 4 FDA reports)
CARPAL TUNNEL SYNDROME ( 4 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CUBITAL TUNNEL SYNDROME ( 4 FDA reports)
DEAFNESS ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DENTAL FISTULA ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DYSMORPHISM ( 4 FDA reports)
EDENTULOUS ( 4 FDA reports)
ELECTROCARDIOGRAM P WAVE ABNORMAL ( 4 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 4 FDA reports)
ELECTROLYTE IMBALANCE ( 4 FDA reports)
EMBOLIC STROKE ( 4 FDA reports)
ENDOPHTHALMITIS ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
FACIAL PAIN ( 4 FDA reports)
FLANK PAIN ( 4 FDA reports)
GANGRENE ( 4 FDA reports)
GAZE PALSY ( 4 FDA reports)
HAEMORRHAGIC INFARCTION ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HEAD AND NECK CANCER ( 4 FDA reports)
HERPES SIMPLEX ( 4 FDA reports)
HYPERLIPIDAEMIA ( 4 FDA reports)
HYPERMETROPIA ( 4 FDA reports)
HYPOMAGNESAEMIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
ILL-DEFINED DISORDER ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INJECTION SITE HAEMORRHAGE ( 4 FDA reports)
INTERSTITIAL LUNG DISEASE ( 4 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 4 FDA reports)
JAW DISORDER ( 4 FDA reports)
JUGULAR VEIN THROMBOSIS ( 4 FDA reports)
LARYNGITIS ( 4 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 4 FDA reports)
LEUKOENCEPHALOPATHY ( 4 FDA reports)
LICHENOID KERATOSIS ( 4 FDA reports)
LIMB DISCOMFORT ( 4 FDA reports)
LOCAL SWELLING ( 4 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 4 FDA reports)
MASS ( 4 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 4 FDA reports)
MOTOR DYSFUNCTION ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
NASAL DISCOMFORT ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
OBESITY ( 4 FDA reports)
OCULAR HYPERTENSION ( 4 FDA reports)
OESOPHAGITIS ULCERATIVE ( 4 FDA reports)
ORAL TORUS ( 4 FDA reports)
OSTEITIS ( 4 FDA reports)
OSTEODYSTROPHY ( 4 FDA reports)
PALATAL DISORDER ( 4 FDA reports)
PARAPLEGIA ( 4 FDA reports)
PEAU D'ORANGE ( 4 FDA reports)
PERICARDITIS ( 4 FDA reports)
PERIODONTAL DISEASE ( 4 FDA reports)
PERITONEAL HAEMORRHAGE ( 4 FDA reports)
PITTING OEDEMA ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PLEURECTOMY ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
POLYURIA ( 4 FDA reports)
POOR SUCKING REFLEX ( 4 FDA reports)
POSTINFARCTION ANGINA ( 4 FDA reports)
PRODUCTIVE COUGH ( 4 FDA reports)
PROSTHESIS USER ( 4 FDA reports)
PSEUDOBULBAR PALSY ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
SEDATION ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SKIN BURNING SENSATION ( 4 FDA reports)
SLEEP APNOEA SYNDROME ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SQUAMOUS CELL CARCINOMA ( 4 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 4 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
TACHYARRHYTHMIA ( 4 FDA reports)
TENDONITIS ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
TONGUE INJURY ( 4 FDA reports)
TONIC CONVULSION ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TYPE 2 DIABETES MELLITUS ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
URINE OUTPUT DECREASED ( 4 FDA reports)
VERBAL ABUSE ( 4 FDA reports)
VISUAL IMPAIRMENT ( 4 FDA reports)
ACCELERATED IDIOVENTRICULAR RHYTHM ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
APGAR SCORE LOW ( 3 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
ARTERIAL THROMBOSIS ( 3 FDA reports)
ARTERIOVENOUS FISTULA THROMBOSIS ( 3 FDA reports)
ARTHROPATHY ( 3 FDA reports)
ASTIGMATISM ( 3 FDA reports)
BLOOD CULTURE POSITIVE ( 3 FDA reports)
BONE DENSITY DECREASED ( 3 FDA reports)
BONE MARROW TRANSPLANT ( 3 FDA reports)
BONE NEOPLASM MALIGNANT ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
BUNDLE BRANCH BLOCK ( 3 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CARDIAC FLUTTER ( 3 FDA reports)
CARDIOVASCULAR DISORDER ( 3 FDA reports)
CARDIOVASCULAR INSUFFICIENCY ( 3 FDA reports)
CATHETER SITE HAEMORRHAGE ( 3 FDA reports)
CEREBELLAR HAEMORRHAGE ( 3 FDA reports)
CEREBRAL DISORDER ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CLOSTRIDIAL INFECTION ( 3 FDA reports)
COMPLEX PARTIAL SEIZURES ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CORONARY ARTERY STENOSIS ( 3 FDA reports)
DERMATITIS ATOPIC ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
EFFUSION ( 3 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 3 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 3 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 3 FDA reports)
ENTEROCUTANEOUS FISTULA ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
EXERCISE TOLERANCE DECREASED ( 3 FDA reports)
FINGER AMPUTATION ( 3 FDA reports)
FOLLICULITIS ( 3 FDA reports)
FUNGAL INFECTION ( 3 FDA reports)
FUNGAL SKIN INFECTION ( 3 FDA reports)
GALLOP RHYTHM PRESENT ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL TOXICITY ( 3 FDA reports)
GOITRE ( 3 FDA reports)
GROIN PAIN ( 3 FDA reports)
HEARING IMPAIRED ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HEPATOMEGALY ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPERKERATOSIS ( 3 FDA reports)
HYPOKINESIA ( 3 FDA reports)
HYPOTHYROIDISM ( 3 FDA reports)
ILEUS ( 3 FDA reports)
INCREASED APPETITE ( 3 FDA reports)
INFECTIOUS DISEASE CARRIER ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LARYNGEAL OEDEMA ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MACULOPATHY ( 3 FDA reports)
MEDICAL DEVICE COMPLICATION ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MIGRAINE ( 3 FDA reports)
MITRAL VALVE INCOMPETENCE ( 3 FDA reports)
MOUTH HAEMORRHAGE ( 3 FDA reports)
MUSCLE CONTRACTURE ( 3 FDA reports)
MUSCULOSKELETAL DISORDER ( 3 FDA reports)
NEPHROLITHIASIS ( 3 FDA reports)
NEUTROPHIL COUNT INCREASED ( 3 FDA reports)
OEDEMA MOUTH ( 3 FDA reports)
PANCREATIC HAEMORRHAGE ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PERIPHERAL EMBOLISM ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PHARYNGITIS ( 3 FDA reports)
PHOTOPSIA ( 3 FDA reports)
POLLAKIURIA ( 3 FDA reports)
POLYCYTHAEMIA ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
POSTURING ( 3 FDA reports)
PRESBYOPIA ( 3 FDA reports)
PURULENT DISCHARGE ( 3 FDA reports)
RESPIRATORY DEPRESSION ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
RESPIRATORY TRACT INFECTION ( 3 FDA reports)
ROSACEA ( 3 FDA reports)
SEBORRHOEIC DERMATITIS ( 3 FDA reports)
SPLENIC ABSCESS ( 3 FDA reports)
SPLENIC INFARCTION ( 3 FDA reports)
SPLENIC INJURY ( 3 FDA reports)
SPUTUM DISCOLOURED ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 3 FDA reports)
SUBDURAL HAEMATOMA ( 3 FDA reports)
SUDDEN DEATH ( 3 FDA reports)
SUFFOCATION FEELING ( 3 FDA reports)
TENDON DISORDER ( 3 FDA reports)
THIRST ( 3 FDA reports)
THROMBOPHLEBITIS SUPERFICIAL ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TINNITUS ( 3 FDA reports)
TROPONIN I INCREASED ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
VAGINITIS BACTERIAL ( 3 FDA reports)
VASCULAR OCCLUSION ( 3 FDA reports)
VENOUS THROMBOSIS ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VITREOUS FLOATERS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL SYMPTOM ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABORTION MISSED ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME SHORTENED ( 2 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN INTESTINE ( 2 FDA reports)
ACUTE LEUKAEMIA ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGONAL RHYTHM ( 2 FDA reports)
ALCOHOL USE ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANAL FISSURE ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ANTIPHOSPHOLIPID ANTIBODIES ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APALLIC SYNDROME ( 2 FDA reports)
ARTERIOVENOUS GRAFT SITE INFECTION ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ARTHROSCOPY ( 2 FDA reports)
ASPIRATION BONE MARROW ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD FIBRINOGEN ABNORMAL ( 2 FDA reports)
BLOOD OSMOLARITY DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRAIN COMPRESSION ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
BUNION ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
CALCULUS URETERIC ( 2 FDA reports)
CARDIAC ENZYMES INCREASED ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 2 FDA reports)
CARDIOMYOPATHY ( 2 FDA reports)
CATHETER RELATED COMPLICATION ( 2 FDA reports)
CATHETER SITE PAIN ( 2 FDA reports)
CENTRAL LINE INFECTION ( 2 FDA reports)
CHANGE OF BOWEL HABIT ( 2 FDA reports)
CHOLECYSTECTOMY ( 2 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CORD BLOOD TRANSPLANT THERAPY ( 2 FDA reports)
CORNEAL OEDEMA ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
CORYNEBACTERIUM INFECTION ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DISABILITY ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EAR PRURITUS ( 2 FDA reports)
ECONOMIC PROBLEM ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ENCEPHALITIS VIRAL ( 2 FDA reports)
ENTEROCOCCAL SEPSIS ( 2 FDA reports)
EPIGASTRIC DISCOMFORT ( 2 FDA reports)
EXOSTOSIS ( 2 FDA reports)
EXTREMITY NECROSIS ( 2 FDA reports)
EYE INFECTION BACTERIAL ( 2 FDA reports)
EYE LASER SURGERY ( 2 FDA reports)
EYELID MARGIN CRUSTING ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOAMING AT MOUTH ( 2 FDA reports)
FUNGAEMIA ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GENERALISED ANXIETY DISORDER ( 2 FDA reports)
GINGIVAL INFECTION ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMOLYTIC ANAEMIA ( 2 FDA reports)
HAND FRACTURE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEMIANOPIA HOMONYMOUS ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATORENAL FAILURE ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERNATRAEMIA ( 2 FDA reports)
HYPERSOMNIA ( 2 FDA reports)
HYPERTENSIVE CRISIS ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCOAGULABLE STATE ( 2 FDA reports)
HYPOGLYCAEMIA ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
HYPOXIC-ISCHAEMIC ENCEPHALOPATHY ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFUSION SITE ERYTHEMA ( 2 FDA reports)
INGUINAL HERNIA ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
IRITIS ( 2 FDA reports)
ISCHAEMIA ( 2 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JAW OPERATION ( 2 FDA reports)
JOINT INJURY ( 2 FDA reports)
KERATOPATHY ( 2 FDA reports)
KIDNEY MALFORMATION ( 2 FDA reports)
KNEE ARTHROPLASTY ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LACTIC ACIDOSIS ( 2 FDA reports)
LEARNING DISORDER ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MENISCUS LESION ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
METABOLIC ENCEPHALOPATHY ( 2 FDA reports)
METAPLASIA ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MOANING ( 2 FDA reports)
MONOCLONAL GAMMOPATHY ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE TWITCHING ( 2 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
MYDRIASIS ( 2 FDA reports)
MYOCARDIAL HAEMORRHAGE ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NICOTINE DEPENDENCE ( 2 FDA reports)
OESOPHAGEAL DILATATION ( 2 FDA reports)
OPERATIVE HAEMORRHAGE ( 2 FDA reports)
OPHTHALMOPLEGIA ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
OVARIAN CYST ( 2 FDA reports)
OXYGEN SATURATION ABNORMAL ( 2 FDA reports)
PARALYSIS FLACCID ( 2 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 2 FDA reports)
PHARYNGEAL HYPOAESTHESIA ( 2 FDA reports)
PHLEBITIS ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLASMACYTOMA ( 2 FDA reports)
PLEURAL HAEMORRHAGE ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
POLYDIPSIA ( 2 FDA reports)
POOR PERIPHERAL CIRCULATION ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
PRECEREBRAL ARTERY OCCLUSION ( 2 FDA reports)
PREMATURE BABY ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROCTALGIA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RADIOTHERAPY ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RETINAL ARTERY OCCLUSION ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
REVERSIBLE POSTERIOR LEUKOENCEPHALOPATHY SYNDROME ( 2 FDA reports)
SALMONELLA SEPSIS ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SERRATIA INFECTION ( 2 FDA reports)
SERUM SICKNESS ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SKIN CANCER ( 2 FDA reports)
SKIN LACERATION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
SOMATISATION DISORDER ( 2 FDA reports)
SPLENIC RUPTURE ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 2 FDA reports)
STEATORRHOEA ( 2 FDA reports)
STREPTOCOCCAL SEPSIS ( 2 FDA reports)
STRESS FRACTURE ( 2 FDA reports)
STRESS URINARY INCONTINENCE ( 2 FDA reports)
SUBCUTANEOUS NODULE ( 2 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 2 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 2 FDA reports)
TINEA PEDIS ( 2 FDA reports)
TONGUE HAEMORRHAGE ( 2 FDA reports)
TREATMENT FAILURE ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TYMPANIC MEMBRANE PERFORATION ( 2 FDA reports)
ULCER ( 2 FDA reports)
UPPER AIRWAY OBSTRUCTION ( 2 FDA reports)
URETHRAL OBSTRUCTION ( 2 FDA reports)
UTERINE LEIOMYOMA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VARICOSE VEIN OPERATION ( 2 FDA reports)
VASCULAR GRAFT THROMBOSIS ( 2 FDA reports)
VENTRICULAR HYPERTROPHY ( 2 FDA reports)
VIITH NERVE PARALYSIS ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
WOUND INFECTION ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
XEROSIS ( 2 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ABDOMINAL RIGIDITY ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN SKIN ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA RECURRENT ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANEURYSM RUPTURED ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
AORTITIS ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ARTERIOVENOUS FISTULA ANEURYSM ( 1 FDA reports)
ARTERIOVENOUS FISTULA SITE COMPLICATION ( 1 FDA reports)
ARTHROFIBROSIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BASAL GANGLIA HAEMORRHAGE ( 1 FDA reports)
BASAL GANGLION DEGENERATION ( 1 FDA reports)
BELLIGERENCE ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD IRON DECREASED ( 1 FDA reports)
BLOOD LACTIC ACID INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD URINE ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BLOODY DISCHARGE ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN STEM SYNDROME ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BUDD-CHIARI SYNDROME ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CAPILLARY LEAK SYNDROME ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIAC OUTPUT INCREASED ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CATARACT SUBCAPSULAR ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CATHETER SITE DISCHARGE ( 1 FDA reports)
CATHETER SITE INFECTION ( 1 FDA reports)
CATHETER SITE RELATED REACTION ( 1 FDA reports)
CEREBRAL ARTERY STENOSIS ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HYPOPERFUSION ( 1 FDA reports)
CEREBRAL THROMBOSIS ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHEMICAL EYE INJURY ( 1 FDA reports)
CHEST INJURY ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOREA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL INCREASED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONJUNCTIVAL HAEMORRHAGE ( 1 FDA reports)
CONTINUOUS HAEMODIAFILTRATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
COR PULMONALE ( 1 FDA reports)
CORNEAL ABRASION ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
COSTOVERTEBRAL ANGLE TENDERNESS ( 1 FDA reports)
CRYING ( 1 FDA reports)
DECOMPRESSION SICKNESS ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DENTURE WEARER ( 1 FDA reports)
DERMATITIS ACNEIFORM ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 1 FDA reports)
DEVELOPMENTAL DELAY ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIABETIC RETINAL OEDEMA ( 1 FDA reports)
DIABETIC RETINOPATHY ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DROOLING ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE PEAKED ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
EMBOLIC CEREBRAL INFARCTION ( 1 FDA reports)
EMBOLISM ARTERIAL ( 1 FDA reports)
ENDOCARDIAL FIBROSIS ( 1 FDA reports)
ENDOTRACHEAL INTUBATION COMPLICATION ( 1 FDA reports)
ENTEROBACTER PNEUMONIA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXFOLIATIVE RASH ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE EXCISION ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID BLEEDING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FAMILY STRESS ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FEMORAL NERVE PALSY ( 1 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 1 FDA reports)
FIBRINOLYSIS ( 1 FDA reports)
FIBRINOUS BRONCHITIS ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL HEART RATE DECELERATION ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTRITIS EROSIVE ( 1 FDA reports)
GASTROINTESTINAL OEDEMA ( 1 FDA reports)
GASTROINTESTINAL STOMA COMPLICATION ( 1 FDA reports)
GENERAL SYMPTOM ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAM STAIN POSITIVE ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
GRANULOMATOUS LIVER DISEASE ( 1 FDA reports)
GUILLAIN-BARRE SYNDROME ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOPNEUMOTHORAX ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HEPATIC CONGESTION ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATIC VEIN THROMBOSIS ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HEREDITARY SPHEROCYTOSIS ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHLORHYDRIA ( 1 FDA reports)
HYPERCOAGULATION ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPOFIBRINOGENAEMIA ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
HYSTERECTOMY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPLANT SITE NECROSIS ( 1 FDA reports)
IMPLANT SITE THROMBOSIS ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA VIRUS TEST POSITIVE ( 1 FDA reports)
INFUSION SITE EXTRAVASATION ( 1 FDA reports)
INFUSION SITE PAIN ( 1 FDA reports)
INFUSION SITE SWELLING ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INGROWING NAIL ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRACRANIAL HAEMATOMA ( 1 FDA reports)
INTUBATION ( 1 FDA reports)
JOINT ANKYLOSIS ( 1 FDA reports)
JOINT DEPOSIT ( 1 FDA reports)
JOINT EFFUSION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KLEBSIELLA TEST POSITIVE ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIP HAEMORRHAGE ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER ABSCESS ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACROGLOSSIA ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MEDIASTINAL HAEMORRHAGE ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENSTRUAL DISORDER ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METASTASES TO PERITONEUM ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MUMPS ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MYOCARDIAL STRAIN ( 1 FDA reports)
MYOCARDIAL STUNNING ( 1 FDA reports)
NASAL SEPTUM DEVIATION ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUTROPENIC INFECTION ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OOPHORECTOMY ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OXYGEN CONSUMPTION INCREASED ( 1 FDA reports)
PAIN EXACERBATED ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PAPILLOEDEMA ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEDAL PULSE DECREASED ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PERFORMANCE STATUS DECREASED ( 1 FDA reports)
PERICARDIAL EFFUSION MALIGNANT ( 1 FDA reports)
PERIPHERAL PULSE DECREASED ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONEAL DISORDER ( 1 FDA reports)
PERITONEAL INFECTION ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHLEBOLITH ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
POLYNEUROPATHY ( 1 FDA reports)
POOR DENTAL CONDITION ( 1 FDA reports)
POST PROCEDURAL DISCHARGE ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST THROMBOTIC SYNDROME ( 1 FDA reports)
POSTOPERATIVE FEVER ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY GRANULOMA ( 1 FDA reports)
PULMONARY MASS ( 1 FDA reports)
PULMONARY VALVE INCOMPETENCE ( 1 FDA reports)
PULSE ABNORMAL ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
PUPILS UNEQUAL ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL CELL CARCINOMA ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL HAEMATOMA ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
REOCCLUSION ( 1 FDA reports)
RESPIRATORY ALKALOSIS ( 1 FDA reports)
RESTRICTIVE CARDIOMYOPATHY ( 1 FDA reports)
RESTRICTIVE PULMONARY DISEASE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETINAL DETACHMENT ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
RIGHT VENTRICULAR SYSTOLIC PRESSURE INCREASED ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEPTIC EMBOLUS ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BACTERIAL INFECTION ( 1 FDA reports)
SKIN FISSURES ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SOCIAL PROBLEM ( 1 FDA reports)
SPINAL CORD OEDEMA ( 1 FDA reports)
SPINAL SHOCK ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STARING ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STREPTOCOCCAL SEROLOGY POSITIVE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUBCLAVIAN VEIN THROMBOSIS ( 1 FDA reports)
SUBDURAL HAEMORRHAGE ( 1 FDA reports)
SUBENDOCARDIAL ISCHAEMIA ( 1 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 1 FDA reports)
SUPRAPUBIC PAIN ( 1 FDA reports)
SURGERY ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TALIPES ( 1 FDA reports)
TARDIVE DYSKINESIA ( 1 FDA reports)
THERAPEUTIC PRODUCT CONTAMINATION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
THYROID HAEMORRHAGE ( 1 FDA reports)
TONGUE BLISTERING ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH SOCKET HAEMORRHAGE ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TRACHEAL DISORDER ( 1 FDA reports)
TRANSMISSION OF AN INFECTIOUS AGENT VIA A MEDICINAL PRODUCT ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICHIASIS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
URINE SODIUM DECREASED ( 1 FDA reports)
UROSEPSIS ( 1 FDA reports)
UTERINE ATROPHY ( 1 FDA reports)
UTERINE HAEMORRHAGE ( 1 FDA reports)
VASCULAR CALCIFICATION ( 1 FDA reports)
VASCULAR HEADACHE ( 1 FDA reports)
VASCULAR RESISTANCE SYSTEMIC DECREASED ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VENIPUNCTURE SITE REACTION ( 1 FDA reports)
VENOOCCLUSIVE DISEASE ( 1 FDA reports)
VENOUS INSUFFICIENCY ( 1 FDA reports)
VENOUS OCCLUSION ( 1 FDA reports)
VENOUS PRESSURE INCREASED ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VESSEL PUNCTURE SITE HAEMATOMA ( 1 FDA reports)
WHITE BLOOD CELL ANALYSIS INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DRAINAGE ( 1 FDA reports)
WOUND HAEMORRHAGE ( 1 FDA reports)
WOUND NECROSIS ( 1 FDA reports)

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