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

DYSPNOEA ( 22 FDA reports)
ABDOMINAL PAIN ( 18 FDA reports)
NAUSEA ( 18 FDA reports)
VOMITING ( 17 FDA reports)
HYPOTENSION ( 13 FDA reports)
PNEUMONIA ( 13 FDA reports)
ASTHENIA ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
HAEMOGLOBIN DECREASED ( 11 FDA reports)
MULTI-ORGAN FAILURE ( 11 FDA reports)
BLOOD CREATININE INCREASED ( 9 FDA reports)
DEHYDRATION ( 9 FDA reports)
MYOCARDIAL INFARCTION ( 9 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
DIARRHOEA ( 8 FDA reports)
DISEASE PROGRESSION ( 8 FDA reports)
HYPERHIDROSIS ( 8 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CHEST PAIN ( 7 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
PALPITATIONS ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
RENAL FAILURE ACUTE ( 7 FDA reports)
VISION BLURRED ( 7 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HYPERKALAEMIA ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
ILEUS ( 6 FDA reports)
LACUNAR INFARCTION ( 6 FDA reports)
PRURITUS ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
BACTERAEMIA ( 5 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CARDIAC TAMPONADE ( 5 FDA reports)
CONSTIPATION ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HYPOVOLAEMIC SHOCK ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
ACIDOSIS ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANGER ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ARRHYTHMIA SUPRAVENTRICULAR ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BLOOD BILIRUBIN INCREASED ( 4 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 4 FDA reports)
CARDIAC DISORDER ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CONVULSION ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
CORONARY ARTERY STENOSIS ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
FEBRILE NEUTROPENIA ( 4 FDA reports)
GASTROENTERITIS ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
IRRITABILITY ( 4 FDA reports)
METABOLIC ALKALOSIS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NEUTROPENIC SEPSIS ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PULMONARY OEDEMA ( 4 FDA reports)
RASH ( 4 FDA reports)
RENAL PAIN ( 4 FDA reports)
SUBILEUS ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BREAST CANCER FEMALE ( 3 FDA reports)
CARDIAC OUTPUT DECREASED ( 3 FDA reports)
CATARACT ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DERMATITIS CONTACT ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
FALL ( 3 FDA reports)
GASTRITIS EROSIVE ( 3 FDA reports)
GLUCOSE URINE PRESENT ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HEPATOTOXICITY ( 3 FDA reports)
HYPOGLYCAEMIA ( 3 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PEPTIC ULCER ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SWELLING ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
TREMOR ( 3 FDA reports)
TUMOUR LYSIS SYNDROME ( 3 FDA reports)
VASCULAR GRAFT OCCLUSION ( 3 FDA reports)
VASOSPASM ( 3 FDA reports)
VENTRICULAR DYSFUNCTION ( 3 FDA reports)
VENTRICULAR HYPERTROPHY ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ALKALOSIS HYPOCHLORAEMIC ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
AORTIC ANEURYSM ( 2 FDA reports)
ARTHROPATHY ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
AUTOIMMUNE DISORDER ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD LACTIC ACID INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BURSITIS ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
CUTANEOUS LUPUS ERYTHEMATOSUS ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
ENURESIS ( 2 FDA reports)
EYE DISCHARGE ( 2 FDA reports)
EYE INFLAMMATION ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
EYE PRURITUS ( 2 FDA reports)
EYE REDNESS ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC DISORDER ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATOCELLULAR DAMAGE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJECTION SITE BURNING ( 2 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LOOSE STOOLS ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MELAENA ( 2 FDA reports)
MITRAL VALVE INCOMPETENCE ( 2 FDA reports)
MITRAL VALVE PROLAPSE ( 2 FDA reports)
MONOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 2 FDA reports)
PAIN ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POST PROCEDURAL PAIN ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RED BLOOD CELLS URINE ( 2 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RETROPERITONEAL HAEMORRHAGE ( 2 FDA reports)
RIGHT VENTRICULAR FAILURE ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN HYPERTROPHY ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPINAL DISORDER ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SYNCOPE VASOVAGAL ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
URINE KETONE BODY PRESENT ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VISUAL IMPAIRMENT ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
WOUND COMPLICATION ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABSCESS JAW ( 1 FDA reports)
ACANTHOLYSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK THIRD DEGREE ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD ZINC DECREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CARDIAC INDEX DECREASED ( 1 FDA reports)
CARDIAC VENTRICULAR DISORDER ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARNITINE DECREASED ( 1 FDA reports)
CATARACT OPERATION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBELLAR HAEMORRHAGE ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COMPLETED SUICIDE ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGESTIVE CARDIOMYOPATHY ( 1 FDA reports)
CONJUNCTIVAL ABRASION ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CORONARY ARTERY ATHEROSCLEROSIS ( 1 FDA reports)
CORONARY OSTIAL STENOSIS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
DEATH ( 1 FDA reports)
DEPRESSION POSTOPERATIVE ( 1 FDA reports)
DERMATITIS PSORIASIFORM ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG EFFECT INCREASED ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR INJURY ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
ENERGY INCREASED ( 1 FDA reports)
ENTEROBACTER INFECTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EXPOSURE TO TOXIC AGENT ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID MARGIN CRUSTING ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FIBROSIS ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOOT FRACTURE ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
FUNGAL RASH ( 1 FDA reports)
FUNGAL SEPSIS ( 1 FDA reports)
FUNGUS SPUTUM TEST POSITIVE ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC CANCER STAGE 0 ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL ULCER ( 1 FDA reports)
GINGIVAL PAIN ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMODYNAMIC INSTABILITY ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEUKOSTASIS ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENOPAUSE ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
NEUROLOGICAL INFECTION ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
NIKOLSKY'S SIGN ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NOSOCOMIAL INFECTION ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONYCHOLYSIS ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
PAIN OF SKIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PEMPHIGUS ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PITUITARY TUMOUR RECURRENT ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
PNEUMOPERITONEUM ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
POST PROCEDURAL HAEMORRHAGE ( 1 FDA reports)
POSTURE ABNORMAL ( 1 FDA reports)
PRIAPISM ( 1 FDA reports)
PROTEIN URINE ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
RADIOISOTOPE SCAN ABNORMAL ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 1 FDA reports)
RETINAL DISORDER ( 1 FDA reports)
RETINAL VEIN THROMBOSIS ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SEROTONIN SYNDROME ( 1 FDA reports)
SERUM FERRITIN DECREASED ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP TALKING ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH FRACTURE ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
UTERINE POLYPECTOMY ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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