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

FALL ( 42 FDA reports)
DYSPNOEA ( 38 FDA reports)
OEDEMA PERIPHERAL ( 36 FDA reports)
RENAL FAILURE ( 36 FDA reports)
ASTHENIA ( 34 FDA reports)
RENAL FAILURE ACUTE ( 32 FDA reports)
CHEST PAIN ( 30 FDA reports)
PAIN IN EXTREMITY ( 29 FDA reports)
CONFUSIONAL STATE ( 28 FDA reports)
PAIN ( 28 FDA reports)
DIARRHOEA ( 27 FDA reports)
DIZZINESS ( 27 FDA reports)
BACK PAIN ( 26 FDA reports)
NAUSEA ( 26 FDA reports)
CARDIAC FAILURE ( 25 FDA reports)
DRUG INEFFECTIVE ( 25 FDA reports)
HYPONATRAEMIA ( 25 FDA reports)
MYOCARDIAL INFARCTION ( 25 FDA reports)
ANXIETY ( 22 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 22 FDA reports)
FATIGUE ( 22 FDA reports)
VOMITING ( 22 FDA reports)
DEPRESSION ( 21 FDA reports)
ARTHRALGIA ( 20 FDA reports)
CELLULITIS ( 19 FDA reports)
CARDIAC DISORDER ( 18 FDA reports)
HYPERKALAEMIA ( 18 FDA reports)
NEUROPATHY PERIPHERAL ( 18 FDA reports)
PNEUMONIA ( 17 FDA reports)
PYREXIA ( 17 FDA reports)
CONSTIPATION ( 16 FDA reports)
DRUG INTERACTION ( 16 FDA reports)
INSOMNIA ( 16 FDA reports)
WEIGHT INCREASED ( 16 FDA reports)
ABDOMINAL DISTENSION ( 15 FDA reports)
CEREBROVASCULAR ACCIDENT ( 15 FDA reports)
DRUG HYPERSENSITIVITY ( 15 FDA reports)
WEIGHT DECREASED ( 15 FDA reports)
ANAEMIA ( 14 FDA reports)
DEATH ( 14 FDA reports)
HEADACHE ( 14 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
CARPAL TUNNEL SYNDROME ( 13 FDA reports)
CATARACT ( 13 FDA reports)
FACIAL PAIN ( 13 FDA reports)
FLUID RETENTION ( 13 FDA reports)
HYPERLIPIDAEMIA ( 13 FDA reports)
INFECTION ( 13 FDA reports)
MUSCULOSKELETAL PAIN ( 13 FDA reports)
PULMONARY HYPERTENSION ( 13 FDA reports)
SWELLING ( 13 FDA reports)
URINARY TRACT INFECTION ( 13 FDA reports)
VISION BLURRED ( 13 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 12 FDA reports)
ATRIAL FIBRILLATION ( 12 FDA reports)
CARDIAC ARREST ( 12 FDA reports)
DIABETIC RETINOPATHY ( 12 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 12 FDA reports)
HYPOAESTHESIA ( 12 FDA reports)
HYPOTENSION ( 12 FDA reports)
LIPOMA ( 12 FDA reports)
TREMOR ( 12 FDA reports)
BLOOD PRESSURE INCREASED ( 11 FDA reports)
BRADYCARDIA ( 11 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 11 FDA reports)
CARDIOMEGALY ( 11 FDA reports)
DECREASED APPETITE ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
DIABETES MELLITUS ( 11 FDA reports)
GINGIVITIS ( 11 FDA reports)
HYPOGLYCAEMIA ( 11 FDA reports)
MALAISE ( 11 FDA reports)
OBESITY ( 11 FDA reports)
PANIC ATTACK ( 11 FDA reports)
RESPIRATORY FAILURE ( 11 FDA reports)
ROTATOR CUFF SYNDROME ( 11 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 11 FDA reports)
ABSCESS LIMB ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
ANGIOLIPOMA ( 10 FDA reports)
ARTHRITIS ( 10 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
BLINDNESS ( 10 FDA reports)
BLOOD CREATININE INCREASED ( 10 FDA reports)
BLOOD UREA INCREASED ( 10 FDA reports)
BONE SARCOMA ( 10 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 10 FDA reports)
COMPLEX REGIONAL PAIN SYNDROME ( 10 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
DIABETIC COMA ( 10 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 10 FDA reports)
EYE HAEMORRHAGE ( 10 FDA reports)
GLUCOSE TOLERANCE DECREASED ( 10 FDA reports)
HUMERUS FRACTURE ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
LOSS OF CONSCIOUSNESS ( 10 FDA reports)
LUMBAR RADICULOPATHY ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
NEPHROPATHY ( 10 FDA reports)
NEUROSIS ( 10 FDA reports)
OPTIC NERVE INJURY ( 10 FDA reports)
OROPHARYNGEAL BLISTERING ( 10 FDA reports)
OSTEOARTHRITIS ( 10 FDA reports)
OSTEOPOROSIS ( 10 FDA reports)
PARTIAL SEIZURES ( 10 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 10 FDA reports)
PHOTOPSIA ( 10 FDA reports)
PNEUMONIA BACTERIAL ( 10 FDA reports)
PNEUMONIA VIRAL ( 10 FDA reports)
RETINAL DETACHMENT ( 10 FDA reports)
RETINAL VASCULAR DISORDER ( 10 FDA reports)
RHEUMATOID ARTHRITIS ( 10 FDA reports)
SINUS HEADACHE ( 10 FDA reports)
SUBCUTANEOUS NODULE ( 10 FDA reports)
SYNOVIAL RUPTURE ( 10 FDA reports)
THERMAL BURN ( 10 FDA reports)
TOOTH LOSS ( 10 FDA reports)
VENTRICULAR FIBRILLATION ( 10 FDA reports)
VITREOUS HAEMORRHAGE ( 10 FDA reports)
ABASIA ( 9 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
CORONARY ARTERY DISEASE ( 9 FDA reports)
COUGH ( 9 FDA reports)
ERYTHEMA ( 9 FDA reports)
FACE OEDEMA ( 9 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
IMPAIRED HEALING ( 9 FDA reports)
MITRAL VALVE INCOMPETENCE ( 9 FDA reports)
OEDEMA ( 9 FDA reports)
ORAL PAIN ( 9 FDA reports)
ORTHOPEDIC PROCEDURE ( 9 FDA reports)
PULMONARY EMBOLISM ( 9 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
BONE DENSITY DECREASED ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DYSPHAGIA ( 8 FDA reports)
FEMUR FRACTURE ( 8 FDA reports)
FOOT DEFORMITY ( 8 FDA reports)
FOOT FRACTURE ( 8 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 8 FDA reports)
LIGAMENT DISORDER ( 8 FDA reports)
LYMPHADENOPATHY ( 8 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 8 FDA reports)
OSTEOMA ( 8 FDA reports)
OSTEOMYELITIS ( 8 FDA reports)
PERIORBITAL HAEMATOMA ( 8 FDA reports)
PIRIFORMIS SYNDROME ( 8 FDA reports)
PRURITUS ( 8 FDA reports)
SLEEP APNOEA SYNDROME ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
TORSADE DE POINTES ( 8 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 8 FDA reports)
VENTRICULAR TACHYCARDIA ( 8 FDA reports)
VERTIGO ( 8 FDA reports)
VITREOUS FLOATERS ( 8 FDA reports)
COMPRESSION FRACTURE ( 7 FDA reports)
GASTRIC ULCER ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
HAEMATEMESIS ( 7 FDA reports)
HEAD INJURY ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
HYPOPHAGIA ( 7 FDA reports)
MEDICATION ERROR ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
PAIN IN JAW ( 7 FDA reports)
PANCREATITIS ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 7 FDA reports)
RADICULAR PAIN ( 7 FDA reports)
RASH ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
THROMBOSIS ( 7 FDA reports)
WHEEZING ( 7 FDA reports)
WOUND ( 7 FDA reports)
ANGINA PECTORIS ( 6 FDA reports)
ASCITES ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
BONE DISORDER ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
COLON CANCER ( 6 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 6 FDA reports)
EOSINOPHILIA ( 6 FDA reports)
GAIT DISTURBANCE ( 6 FDA reports)
GINGIVAL BLEEDING ( 6 FDA reports)
HYDRONEPHROSIS ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LOOSE BODY IN JOINT ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
METATARSALGIA ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
NASOPHARYNGITIS ( 6 FDA reports)
NECK PAIN ( 6 FDA reports)
ORTHOSTATIC HYPOTENSION ( 6 FDA reports)
OSTEONECROSIS OF JAW ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
PERICARDIAL EFFUSION ( 6 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 6 FDA reports)
PLATELET COUNT INCREASED ( 6 FDA reports)
PRIMARY SEQUESTRUM ( 6 FDA reports)
SCIATICA ( 6 FDA reports)
SINUS BRADYCARDIA ( 6 FDA reports)
SINUSITIS ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SURGERY ( 6 FDA reports)
TUBERCULIN TEST POSITIVE ( 6 FDA reports)
TUBERCULOSIS ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ABSCESS ORAL ( 5 FDA reports)
ALOPECIA ( 5 FDA reports)
ARTHROPATHY ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 5 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 5 FDA reports)
BLOOD GLUCOSE DECREASED ( 5 FDA reports)
CARDIO-RESPIRATORY ARREST ( 5 FDA reports)
CIRCULATORY COLLAPSE ( 5 FDA reports)
CLAVICLE FRACTURE ( 5 FDA reports)
COMA ( 5 FDA reports)
CYST ( 5 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 5 FDA reports)
DISORIENTATION ( 5 FDA reports)
DRY MOUTH ( 5 FDA reports)
EMOTIONAL DISTRESS ( 5 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 5 FDA reports)
FIBROSIS ( 5 FDA reports)
GINGIVAL OEDEMA ( 5 FDA reports)
GYNAECOMASTIA ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HEPATIC ENZYME INCREASED ( 5 FDA reports)
HYPOCHLORAEMIA ( 5 FDA reports)
HYPOTHYROIDISM ( 5 FDA reports)
INDURATION ( 5 FDA reports)
IRRITABLE BOWEL SYNDROME ( 5 FDA reports)
JAW FRACTURE ( 5 FDA reports)
KIDNEY INFECTION ( 5 FDA reports)
METASTASES TO BONE ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
PLEURAL FIBROSIS ( 5 FDA reports)
POLYP COLORECTAL ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
PULSE ABSENT ( 5 FDA reports)
REGURGITATION ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
SWELLING FACE ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
THROMBOCYTOPENIA ( 5 FDA reports)
TOOTH EXTRACTION ( 5 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 5 FDA reports)
TRISMUS ( 5 FDA reports)
TYPE 2 DIABETES MELLITUS ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
URINARY INCONTINENCE ( 5 FDA reports)
VENTRICULAR ARRHYTHMIA ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ALVEOLOPLASTY ( 4 FDA reports)
APLASIA PURE RED CELL ( 4 FDA reports)
ASPIRATION ( 4 FDA reports)
BALANCE DISORDER ( 4 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BONE DEBRIDEMENT ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
CENTRAL VENOUS CATHETER REMOVAL ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CLOSTRIDIAL INFECTION ( 4 FDA reports)
DENTAL PROSTHESIS PLACEMENT ( 4 FDA reports)
DEVICE RELATED INFECTION ( 4 FDA reports)
DILATATION ATRIAL ( 4 FDA reports)
DIPLOPIA ( 4 FDA reports)
DIVERTICULUM ( 4 FDA reports)
ECONOMIC PROBLEM ( 4 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 4 FDA reports)
ENTEROCOCCAL INFECTION ( 4 FDA reports)
EPISTAXIS ( 4 FDA reports)
EXTRASYSTOLES ( 4 FDA reports)
HEPATIC STEATOSIS ( 4 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 4 FDA reports)
HYPERCALCAEMIA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
HYPOVOLAEMIA ( 4 FDA reports)
IMPAIRED WORK ABILITY ( 4 FDA reports)
INCISIONAL DRAINAGE ( 4 FDA reports)
INFUSION RELATED REACTION ( 4 FDA reports)
INJURY ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
JAW OPERATION ( 4 FDA reports)
LEUKOCYTOSIS ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MULTIPLE MYELOMA ( 4 FDA reports)
OESOPHAGITIS ( 4 FDA reports)
ORAL SURGERY ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
PULMONARY ARTERIAL HYPERTENSION ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
SEPSIS ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SPLENOMEGALY ( 4 FDA reports)
TENDON RUPTURE ( 4 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 4 FDA reports)
TOOTH ABSCESS ( 4 FDA reports)
TRACHEOBRONCHITIS ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
UPPER LIMB FRACTURE ( 4 FDA reports)
URINARY RETENTION ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANAPHYLACTOID SHOCK ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
ATAXIA ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 3 FDA reports)
BLOOD PRESSURE IMMEASURABLE ( 3 FDA reports)
BLOODY DISCHARGE ( 3 FDA reports)
BREAST MASS ( 3 FDA reports)
BRONCHIAL CARCINOMA ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CHEMOTHERAPY ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DIABETIC NEUROPATHY ( 3 FDA reports)
DIALYSIS ( 3 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
DYSSTASIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
EAR PAIN ( 3 FDA reports)
ECCHYMOSIS ( 3 FDA reports)
EJECTION FRACTION DECREASED ( 3 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ESCHERICHIA INFECTION ( 3 FDA reports)
EXOSTOSIS ( 3 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 3 FDA reports)
EYE SWELLING ( 3 FDA reports)
FAECALOMA ( 3 FDA reports)
FAILURE TO THRIVE ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 3 FDA reports)
JOINT INSTABILITY ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LUNG DISORDER ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MELAENA ( 3 FDA reports)
METASTATIC PAIN ( 3 FDA reports)
MULTIPLE INJURIES ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
OROPHARYNGEAL PAIN ( 3 FDA reports)
OXYGEN SATURATION DECREASED ( 3 FDA reports)
PANCREATITIS RELAPSING ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PATHOLOGICAL FRACTURE ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PILOERECTION ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RASH PUSTULAR ( 3 FDA reports)
RECTAL HAEMORRHAGE ( 3 FDA reports)
REFLUX OESOPHAGITIS ( 3 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 3 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCAR ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SKIN DISCOLOURATION ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
URINE ABNORMALITY ( 3 FDA reports)
WOUND SECRETION ( 3 FDA reports)
ABDOMINAL HAEMATOMA ( 2 FDA reports)
ABDOMINAL MASS ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 2 FDA reports)
ACANTHOLYSIS ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ADDISON'S DISEASE ( 2 FDA reports)
ADENOCARCINOMA PANCREAS ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
AORTIC VALVE INCOMPETENCE ( 2 FDA reports)
AORTIC VALVE SCLEROSIS ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE PRURITUS ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
ATRIAL FLUTTER ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLADDER SUSPENSION ( 2 FDA reports)
BLINDNESS UNILATERAL ( 2 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 2 FDA reports)
BLOOD DISORDER ( 2 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 2 FDA reports)
BLOOD MERCURY ABNORMAL ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CARCINOID TUMOUR PULMONARY ( 2 FDA reports)
CARDIAC CIRRHOSIS ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIOPULMONARY FAILURE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHOLECYSTITIS ACUTE ( 2 FDA reports)
COAGULATION TIME ABNORMAL ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COELIAC DISEASE ( 2 FDA reports)
COLITIS ( 2 FDA reports)
COLON OPERATION ( 2 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 2 FDA reports)
COR PULMONALE CHRONIC ( 2 FDA reports)
CUSHING'S SYNDROME ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DEAFNESS UNILATERAL ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
DEVELOPMENTAL DELAY ( 2 FDA reports)
DEVICE MALFUNCTION ( 2 FDA reports)
DIABETIC GASTROPARESIS ( 2 FDA reports)
DIAPHRAGMATIC HERNIA ( 2 FDA reports)
DILATATION VENTRICULAR ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DIZZINESS POSTURAL ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DUODENITIS ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EAR DISCOMFORT ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 2 FDA reports)
ELECTROLYTE IMBALANCE ( 2 FDA reports)
ERYSIPELAS ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FLIGHT OF IDEAS ( 2 FDA reports)
FLUID INTAKE REDUCED ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC NEOPLASM ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLAUCOMA ( 2 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPATIC CIRRHOSIS ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERCALCAEMIA OF MALIGNANCY ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERCREATININAEMIA ( 2 FDA reports)
HYPERTENSIVE CARDIOMYOPATHY ( 2 FDA reports)
HYPERTENSIVE HEART DISEASE ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
IMPETIGO ( 2 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INTERCOSTAL NEURALGIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTERVERTEBRAL DISC SPACE NARROWING ( 2 FDA reports)
INTESTINAL FISTULA ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
JOINT LOCK ( 2 FDA reports)
KETOACIDOSIS ( 2 FDA reports)
LARYNGEAL OEDEMA ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LUMBAR SPINAL STENOSIS ( 2 FDA reports)
MASTECTOMY ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MIDDLE EAR EFFUSION ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYODESOPSIA ( 2 FDA reports)
NASAL DRYNESS ( 2 FDA reports)
NEOPLASM ( 2 FDA reports)
NEOPLASM SKIN ( 2 FDA reports)
NERVOUSNESS ( 2 FDA reports)
NIPPLE PAIN ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
OPEN FRACTURE ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OXYGEN SUPPLEMENTATION ( 2 FDA reports)
PACKED RED BLOOD CELL TRANSFUSION ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 2 FDA reports)
PEMPHIGUS ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 2 FDA reports)
POLYNEUROPATHY ( 2 FDA reports)
POST PROCEDURAL COMPLICATION ( 2 FDA reports)
PROTEIN-LOSING GASTROENTEROPATHY ( 2 FDA reports)
PROTEINURIA ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RADICULAR SYNDROME ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RENAL TUBULAR NECROSIS ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESTLESS LEGS SYNDROME ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RETROPERITONEAL HAEMATOMA ( 2 FDA reports)
RHABDOMYOLYSIS ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SCLERODERMA ( 2 FDA reports)
SELF-MEDICATION ( 2 FDA reports)
SEROTONIN SYNDROME ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SHOULDER PAIN ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
SPINAL DECOMPRESSION ( 2 FDA reports)
SPINAL OSTEOARTHRITIS ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 2 FDA reports)
THERAPY NON-RESPONDER ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
ULCER HAEMORRHAGE ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VARICOSE VEIN ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABDOMINAL WALL MASS ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACQUIRED DIAPHRAGMATIC EVENTRATION ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ACUTE HEPATIC FAILURE ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AKATHISIA ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANKLE FRACTURE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
APLASIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE DERMATITIS ( 1 FDA reports)
APPLICATION SITE DESQUAMATION ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 1 FDA reports)
ASEPTIC NECROSIS BONE ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIAL DISEASE CARRIER ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER DILATATION ( 1 FDA reports)
BLADDER OPERATION ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM ABNORMAL ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE CYST ( 1 FDA reports)
BONE EROSION ( 1 FDA reports)
BONE LOSS ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CAFFEINE CONSUMPTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARBON DIOXIDE DECREASED ( 1 FDA reports)
CARDIAC FAILURE ACUTE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOTOXICITY ( 1 FDA reports)
CARTILAGE INJURY ( 1 FDA reports)
CATHETER SITE HAEMATOMA ( 1 FDA reports)
CEREBELLAR SYNDROME ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL SMALL VESSEL ISCHAEMIC DISEASE ( 1 FDA reports)
CERVICAL CYST ( 1 FDA reports)
CHAPPED LIPS ( 1 FDA reports)
CHEST WALL PAIN ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COAGULATION TIME PROLONGED ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLITIS MICROSCOPIC ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONJUNCTIVITIS BACTERIAL ( 1 FDA reports)
CONTRAST MEDIA ALLERGY ( 1 FDA reports)
COOMBS DIRECT TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY EMBOLISM ( 1 FDA reports)
CRYING ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
DECREASED INTEREST ( 1 FDA reports)
DEFORMITY ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DIABETIC GASTROPATHY ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DYSLIPIDAEMIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSTONIA ( 1 FDA reports)
EARLY MORNING AWAKENING ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE ABNORMAL ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
ENDOMETRIAL CANCER ( 1 FDA reports)
ENDOTRACHEAL INTUBATION ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIGASTRIC DISCOMFORT ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 1 FDA reports)
EXTREMITY NECROSIS ( 1 FDA reports)
EYE INFECTION VIRAL ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAECES PALE ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBULA FRACTURE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FOOT AMPUTATION ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HALLUCINATION, TACTILE ( 1 FDA reports)
HEART DISEASE CONGENITAL ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CYST ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HILAR LYMPHADENOPATHY ( 1 FDA reports)
HIP FRACTURE ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HODGKIN'S DISEASE STAGE III ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERMETROPIA ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERURICAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHOLESTEROLAEMIA ( 1 FDA reports)
HYPOGLYCAEMIC COMA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRACRANIAL INJURY ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT CREPITATION ( 1 FDA reports)
JOINT DESTRUCTION ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LIFE EXPECTANCY SHORTENED ( 1 FDA reports)
LIGAMENT INJURY ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIP DRY ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASKED FACIES ( 1 FDA reports)
MASTICATION DISORDER ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDIASTINAL FIBROSIS ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MINI MENTAL STATUS EXAMINATION ABNORMAL ( 1 FDA reports)
MITRAL VALVE DISEASE ( 1 FDA reports)
MIXED LIVER INJURY ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUCOSAL EROSION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYELOCYTOSIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRECTOMY ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOSCLEROSIS ( 1 FDA reports)
OVARIAN CANCER ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONIAN REST TREMOR ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PEPTIC ULCER ( 1 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
PERIPHERAL MOTOR NEUROPATHY ( 1 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PO2 INCREASED ( 1 FDA reports)
PORPHYRIA ( 1 FDA reports)
POSTMENOPAUSAL HAEMORRHAGE ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY BULLA ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RETICULOCYTOSIS ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RETROPERITONEAL FIBROSIS ( 1 FDA reports)
ROTATOR CUFF REPAIR ( 1 FDA reports)
SALIVA ALTERED ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SEBORRHOEIC KERATOSIS ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
SPINAL DISORDER ( 1 FDA reports)
SPONDYLOLISTHESIS ( 1 FDA reports)
SPONTANEOUS HAEMATOMA ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 1 FDA reports)
TENDON INJURY ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOCYTOSIS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TORTICOLLIS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRANSFERRIN SATURATION DECREASED ( 1 FDA reports)
TRANSPLANT FAILURE ( 1 FDA reports)
TRAUMATIC HAEMATOMA ( 1 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINE OUTPUT INCREASED ( 1 FDA reports)
VENOUS STASIS ( 1 FDA reports)
VENOUS THROMBOSIS LIMB ( 1 FDA reports)
VENTRICULAR HYPOKINESIA ( 1 FDA reports)
VERTEBRAL FORAMINAL STENOSIS ( 1 FDA reports)
VIRAL DIARRHOEA ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)
YAWNING ( 1 FDA reports)

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