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

HYPONATRAEMIA ( 46 FDA reports)
RENAL FAILURE ACUTE ( 45 FDA reports)
DRUG INTERACTION ( 39 FDA reports)
NAUSEA ( 34 FDA reports)
VOMITING ( 26 FDA reports)
ABDOMINAL PAIN ( 23 FDA reports)
DIARRHOEA ( 23 FDA reports)
HYPERKALAEMIA ( 22 FDA reports)
ASTHENIA ( 21 FDA reports)
PNEUMONIA ( 21 FDA reports)
HYPOKALAEMIA ( 20 FDA reports)
OEDEMA PERIPHERAL ( 20 FDA reports)
DIZZINESS ( 19 FDA reports)
PYREXIA ( 19 FDA reports)
LACTIC ACIDOSIS ( 18 FDA reports)
CARDIAC ARREST ( 16 FDA reports)
FALL ( 16 FDA reports)
SOMNOLENCE ( 14 FDA reports)
SYNCOPE ( 14 FDA reports)
CONFUSIONAL STATE ( 13 FDA reports)
HYPOCALCAEMIA ( 13 FDA reports)
HYPOTENSION ( 13 FDA reports)
CEREBROVASCULAR ACCIDENT ( 12 FDA reports)
MALAISE ( 12 FDA reports)
PRURITUS ( 12 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
LOSS OF CONSCIOUSNESS ( 11 FDA reports)
VERTIGO ( 11 FDA reports)
CONSTIPATION ( 10 FDA reports)
HYPERTENSION ( 10 FDA reports)
OSTEONECROSIS ( 10 FDA reports)
PAIN IN EXTREMITY ( 10 FDA reports)
RENAL FAILURE CHRONIC ( 10 FDA reports)
VISION BLURRED ( 10 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 9 FDA reports)
ANAEMIA ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
HYPERHIDROSIS ( 9 FDA reports)
HYPOGLYCAEMIA ( 9 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 9 FDA reports)
JOINT SWELLING ( 9 FDA reports)
METABOLIC ACIDOSIS ( 9 FDA reports)
OESOPHAGEAL HAEMORRHAGE ( 9 FDA reports)
AGITATION ( 8 FDA reports)
ARTHROPATHY ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
DEAFNESS UNILATERAL ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HEPATITIS C ( 8 FDA reports)
HERNIA ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 8 FDA reports)
VARICES OESOPHAGEAL ( 8 FDA reports)
BACK PAIN ( 7 FDA reports)
BLOOD CREATININE INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BONE DENSITY DECREASED ( 7 FDA reports)
CARPAL TUNNEL SYNDROME ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
CIRCULATORY COLLAPSE ( 7 FDA reports)
CORONARY ARTERY DISEASE ( 7 FDA reports)
DEPRESSION ( 7 FDA reports)
DIABETES MELLITUS ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
INTERMITTENT CLAUDICATION ( 7 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
OSTEOPOROSIS ( 7 FDA reports)
RASH ( 7 FDA reports)
SPINAL COMPRESSION FRACTURE ( 7 FDA reports)
SPINAL FRACTURE ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ACUTE PRERENAL FAILURE ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BLOOD PRESSURE INCREASED ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 6 FDA reports)
DRUG ABUSE ( 6 FDA reports)
DYSARTHRIA ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
MUSCLE SPASMS ( 6 FDA reports)
RENAL INJURY ( 6 FDA reports)
SLEEP DISORDER ( 6 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TREMOR ( 6 FDA reports)
ALOPECIA ( 5 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 5 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
COLITIS ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
CUBITAL TUNNEL SYNDROME ( 5 FDA reports)
EPICONDYLITIS ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HYPERTENSIVE CRISIS ( 5 FDA reports)
HYPOALBUMINAEMIA ( 5 FDA reports)
HYPOFIBRINOGENAEMIA ( 5 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 5 FDA reports)
LIGAMENT SPRAIN ( 5 FDA reports)
LIPASE INCREASED ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PAIN ( 5 FDA reports)
PALPITATIONS ( 5 FDA reports)
PRESYNCOPE ( 5 FDA reports)
PSORIASIS ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
TACHYCARDIA ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 4 FDA reports)
BARRETT'S OESOPHAGUS ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD OSMOLARITY DECREASED ( 4 FDA reports)
BLOOD POTASSIUM INCREASED ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
COMA ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG LEVEL INCREASED ( 4 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
FLUID RETENTION ( 4 FDA reports)
GAMBLING ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATOTOXICITY ( 4 FDA reports)
HYPERPHOSPHATAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
INFECTION ( 4 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
OVERDOSE ( 4 FDA reports)
RENAL IMPAIRMENT ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ALVEOLITIS ( 3 FDA reports)
AMMONIA INCREASED ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
ATROPHY ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLINDNESS TRANSIENT ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BREAST CANCER RECURRENT ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DIABETIC NEPHROPATHY ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DISEASE PROGRESSION ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DRUG-INDUCED LIVER INJURY ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
DYSPEPSIA ( 3 FDA reports)
DYSPHONIA ( 3 FDA reports)
DYSPHORIA ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 3 FDA reports)
GINGIVAL SWELLING ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
HYPOCHLORAEMIA ( 3 FDA reports)
HYPOPHOSPHATAEMIA ( 3 FDA reports)
HYPOPITUITARISM ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OBESITY ( 3 FDA reports)
OVARIAN ENLARGEMENT ( 3 FDA reports)
OVARIAN NEOPLASM ( 3 FDA reports)
PELVIC FRACTURE ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 3 FDA reports)
PULMONARY FIBROSIS ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 3 FDA reports)
RESTLESS LEGS SYNDROME ( 3 FDA reports)
SEROTONIN SYNDROME ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
THIRST ( 3 FDA reports)
TOOTH ABSCESS ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
UTERINE POLYP ( 3 FDA reports)
VAGINAL DYSPLASIA ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ALCOHOL INTERACTION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGINA PECTORIS ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BONE MARROW DEPRESSION ( 2 FDA reports)
BRACHIAL PLEXUS INJURY ( 2 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRAIN NEOPLASM MALIGNANT ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 2 FDA reports)
CARDIOACTIVE DRUG LEVEL INCREASED ( 2 FDA reports)
CERVICAL SPINE FLATTENING ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
CRYING ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DACRYOSTENOSIS ACQUIRED ( 2 FDA reports)
DEATH ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ENDARTERECTOMY ( 2 FDA reports)
ENDOCRINE DISORDER ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
EYE INFECTION ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HIP FRACTURE ( 2 FDA reports)
HOT FLUSH ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
ISCHAEMIC STROKE ( 2 FDA reports)
JAW DISORDER ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LONG QT SYNDROME ( 2 FDA reports)
MAJOR DEPRESSION ( 2 FDA reports)
MELANOCYTIC NAEVUS ( 2 FDA reports)
MENTAL STATUS CHANGES ( 2 FDA reports)
METASTASES TO LIVER ( 2 FDA reports)
METRORRHAGIA ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OPTIC NERVE DISORDER ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PARKINSONISM ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RENAL TUBULAR DISORDER ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
STASIS DERMATITIS ( 2 FDA reports)
STATUS EPILEPTICUS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
THROMBOCYTOSIS ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABORTION COMPLETE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 1 FDA reports)
ADRENAL CARCINOMA ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
AGRAPHIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANGIOGRAM ( 1 FDA reports)
ANGIOPLASTY ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPLICATION SITE EROSION ( 1 FDA reports)
APPLICATION SITE ERYTHEMA ( 1 FDA reports)
APPLICATION SITE OEDEMA ( 1 FDA reports)
APPLICATION SITE SCAB ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATHEROSCLEROSIS OBLITERANS ( 1 FDA reports)
ATRIAL HYPERTROPHY ( 1 FDA reports)
ATRIAL THROMBOSIS ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AZOTAEMIA ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACTERIA URINE IDENTIFIED ( 1 FDA reports)
BALANITIS ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BUNDLE BRANCH BLOCK ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CENTRAL PONTINE MYELINOLYSIS ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL TOXOPLASMOSIS ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREATININE URINE DECREASED ( 1 FDA reports)
CULTURE POSITIVE ( 1 FDA reports)
CYSTITIS NONINFECTIVE ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DEVICE COLOUR ISSUE ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOPHTHALMITIS ( 1 FDA reports)
ENDOSCOPY ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXTRAVASATION ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID INTAKE RESTRICTION ( 1 FDA reports)
FOOT DEFORMITY ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL PERFORATION ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPLEGIA ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HORMONE LEVEL ABNORMAL ( 1 FDA reports)
HYPERAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERLIPIDAEMIA ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPARATHYROIDISM ( 1 FDA reports)
HYPERTENSIVE NEPHROPATHY ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IATROGENIC INJURY ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
IMPLANTABLE DEFIBRILLATOR INSERTION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INCREASED BRONCHIAL SECRETION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL INFARCTION ( 1 FDA reports)
INTESTINAL ISCHAEMIA ( 1 FDA reports)
INTRACARDIAC MASS ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
ISCHAEMIC HEPATITIS ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT ARTHROPLASTY ( 1 FDA reports)
JOINT SURGERY ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LISTLESS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METABOLIC SYNDROME ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MYCOBACTERIUM AVIUM COMPLEX INFECTION ( 1 FDA reports)
MYCOBACTERIUM FORTUITUM INFECTION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NODULE ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OBLITERATIVE BRONCHIOLITIS ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARATHYROID TUMOUR BENIGN ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PHIMOSIS ( 1 FDA reports)
PITYRIASIS ROSEA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA STREPTOCOCCAL ( 1 FDA reports)
PNEUMONIA VIRAL ( 1 FDA reports)
POLYARTHRITIS ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
PRESCRIPTION FORM TAMPERING ( 1 FDA reports)
PRODUCT FORMULATION ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER METASTATIC ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINOPATHY ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RHEUMATOID NODULE ( 1 FDA reports)
SALIVARY DUCT OBSTRUCTION ( 1 FDA reports)
SALIVARY GLAND CALCULUS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCINTILLATING SCOTOMA ( 1 FDA reports)
SELF-INDUCED VOMITING ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN EROSION ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SMALL CELL LUNG CANCER STAGE UNSPECIFIED ( 1 FDA reports)
SPINAL CORD COMPRESSION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL SEPSIS ( 1 FDA reports)
STRESS CARDIOMYOPATHY ( 1 FDA reports)
STUPOR ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SUPERIOR VENA CAVAL OCCLUSION ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SUTURE RELATED COMPLICATION ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE BITING ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UPPER LIMB FRACTURE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VARICOSE VEIN ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND DEHISCENCE ( 1 FDA reports)

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