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

CONFUSIONAL STATE ( 65 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 64 FDA reports)
ANAEMIA ( 38 FDA reports)
RENAL FAILURE ACUTE ( 37 FDA reports)
VOMITING ( 36 FDA reports)
FALL ( 33 FDA reports)
THROMBOCYTOPENIA ( 33 FDA reports)
ASTHENIA ( 32 FDA reports)
PYREXIA ( 31 FDA reports)
DYSPNOEA ( 29 FDA reports)
DRUG INTERACTION ( 27 FDA reports)
RENAL FAILURE ( 24 FDA reports)
HYPOTENSION ( 23 FDA reports)
NEUTROPENIA ( 22 FDA reports)
SOMNOLENCE ( 22 FDA reports)
CYTOLYTIC HEPATITIS ( 21 FDA reports)
COMA ( 19 FDA reports)
DIARRHOEA ( 19 FDA reports)
DISEASE PROGRESSION ( 18 FDA reports)
RASH MACULO-PAPULAR ( 18 FDA reports)
DEHYDRATION ( 17 FDA reports)
PLEURAL EFFUSION ( 17 FDA reports)
SEPSIS ( 17 FDA reports)
HYPONATRAEMIA ( 16 FDA reports)
MALAISE ( 16 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 16 FDA reports)
NAUSEA ( 16 FDA reports)
ABDOMINAL PAIN ( 15 FDA reports)
BLOOD CREATININE INCREASED ( 15 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 15 FDA reports)
BACK PAIN ( 13 FDA reports)
BALANCE DISORDER ( 13 FDA reports)
CONSTIPATION ( 13 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
STEVENS-JOHNSON SYNDROME ( 13 FDA reports)
CHOLESTASIS ( 12 FDA reports)
DISORIENTATION ( 12 FDA reports)
FACE OEDEMA ( 12 FDA reports)
FATIGUE ( 12 FDA reports)
HALLUCINATION ( 12 FDA reports)
INFLAMMATION ( 12 FDA reports)
ODYNOPHAGIA ( 12 FDA reports)
OVERDOSE ( 12 FDA reports)
SHOCK ( 12 FDA reports)
ANOREXIA ( 11 FDA reports)
OEDEMA ( 11 FDA reports)
OEDEMA PERIPHERAL ( 11 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
DISTURBANCE IN ATTENTION ( 10 FDA reports)
PRURITUS ( 10 FDA reports)
RHABDOMYOLYSIS ( 10 FDA reports)
TOXIC SKIN ERUPTION ( 10 FDA reports)
TREMOR ( 10 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 9 FDA reports)
DRUG ERUPTION ( 9 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 9 FDA reports)
HYPERKALAEMIA ( 9 FDA reports)
LEUKOCYTOSIS ( 9 FDA reports)
RESPIRATORY DISTRESS ( 9 FDA reports)
ABDOMINAL PAIN UPPER ( 8 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
MIOSIS ( 8 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
AMNESIA ( 7 FDA reports)
BONE MARROW FAILURE ( 7 FDA reports)
CELL DEATH ( 7 FDA reports)
CHILLS ( 7 FDA reports)
DECREASED APPETITE ( 7 FDA reports)
EPISTAXIS ( 7 FDA reports)
FEBRILE BONE MARROW APLASIA ( 7 FDA reports)
HAEMOTHORAX ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
INFECTION ( 7 FDA reports)
INTERSTITIAL LUNG DISEASE ( 7 FDA reports)
LEUKOPENIA ( 7 FDA reports)
LUNG DISORDER ( 7 FDA reports)
MELAENA ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
PAIN ( 7 FDA reports)
PELVIC FRACTURE ( 7 FDA reports)
PERICARDIAL EFFUSION ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
FEBRILE NEUTROPENIA ( 6 FDA reports)
HAEMATOMA ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MULTI-ORGAN FAILURE ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
MYOCLONUS ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PETECHIAE ( 6 FDA reports)
TACHYCARDIA ( 6 FDA reports)
URINARY RETENTION ( 6 FDA reports)
URINARY TRACT INFECTION ( 6 FDA reports)
AGITATION ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ANXIETY ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
CONJUNCTIVITIS ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
ECZEMA ( 5 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 5 FDA reports)
HEPATOMEGALY ( 5 FDA reports)
ORAL MUCOSAL ERUPTION ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
PURPURA ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
VERTIGO ( 5 FDA reports)
ABNORMAL BEHAVIOUR ( 4 FDA reports)
ANGIOEDEMA ( 4 FDA reports)
ANURIA ( 4 FDA reports)
APLASIA ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BLOOD PRESSURE INCREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CEREBELLAR SYNDROME ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DRUG PRESCRIBING ERROR ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
EOSINOPHILIA ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
HAEMOLYSIS ( 4 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 4 FDA reports)
HEPATIC ENCEPHALOPATHY ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATITIS CHOLESTATIC ( 4 FDA reports)
HUNGER ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOALBUMINAEMIA ( 4 FDA reports)
HYPOGLYCAEMIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOTHERMIA ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
INFECTED SKIN ULCER ( 4 FDA reports)
JOINT SWELLING ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
LOCKED-IN SYNDROME ( 4 FDA reports)
MALNUTRITION ( 4 FDA reports)
MECHANICAL VENTILATION ( 4 FDA reports)
MUCOSAL INFLAMMATION ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PELVIC VENOUS THROMBOSIS ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
POLYSEROSITIS ( 4 FDA reports)
PREMATURE BABY ( 4 FDA reports)
PROSTHESIS IMPLANTATION ( 4 FDA reports)
PSORIASIS ( 4 FDA reports)
RASH ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
SINUS BRADYCARDIA ( 4 FDA reports)
TRANSAMINASES INCREASED ( 4 FDA reports)
ACUTE HEPATIC FAILURE ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ASPHYXIA ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
CACHEXIA ( 3 FDA reports)
CATHETER RELATED INFECTION ( 3 FDA reports)
CLONUS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG INTOLERANCE ( 3 FDA reports)
DYSAESTHESIA ( 3 FDA reports)
ENCEPHALOPATHY ( 3 FDA reports)
ENDOCARDITIS ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GRAND MAL CONVULSION ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMODIALYSIS ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HAEMORRHAGE ( 3 FDA reports)
HAEMORRHOIDS ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATOCELLULAR INJURY ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERNATRAEMIA ( 3 FDA reports)
HYPOREFLEXIA ( 3 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 3 FDA reports)
INFANTILE SPASMS ( 3 FDA reports)
INFUSION RELATED REACTION ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LYMPHOPENIA ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
NIGHTMARE ( 3 FDA reports)
OPEN WOUND ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
OSTEONECROSIS ( 3 FDA reports)
OVARIAN CANCER ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PANCREATITIS ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PIERRE ROBIN SYNDROME ( 3 FDA reports)
PLEURISY ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
RESPIRATORY DISORDER ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
SKIN LESION ( 3 FDA reports)
SKIN NECROSIS ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SPINAL COMPRESSION FRACTURE ( 3 FDA reports)
STOMATITIS ( 3 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 3 FDA reports)
THORACIC CAVITY DRAINAGE ( 3 FDA reports)
TRANSFUSION REACTION ( 3 FDA reports)
TRAUMATIC HAEMATOMA ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
WOUND ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ALVEOLITIS ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
AREFLEXIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BACTERIAL SEPSIS ( 2 FDA reports)
BLOOD VISCOSITY INCREASED ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BRONCHIAL OBSTRUCTION ( 2 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CARDIOSPASM ( 2 FDA reports)
CEREBRAL ATROPHY ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CLOSTRIDIUM COLITIS ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
DECEREBRATION ( 2 FDA reports)
DELIRIUM ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ENTERAL NUTRITION ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FAECALOMA ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLUID REPLACEMENT ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRIC MUCOSAL LESION ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
HAEMARTHROSIS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEAT THERAPY ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HYPERCAPNIA ( 2 FDA reports)
HYPERTHERMIA ( 2 FDA reports)
HYPOPROTHROMBINAEMIA ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
HYPOVENTILATION ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCREASED BRONCHIAL SECRETION ( 2 FDA reports)
INDURATION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTUBATION ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT SPRAIN ( 2 FDA reports)
LIMB INJURY ( 2 FDA reports)
MALLORY-WEISS SYNDROME ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENTAL DISORDER ( 2 FDA reports)
METASTATIC GASTRIC CANCER ( 2 FDA reports)
METASTATIC NEOPLASM ( 2 FDA reports)
MICROCYTIC ANAEMIA ( 2 FDA reports)
MONOPLEGIA ( 2 FDA reports)
MUSCLE DISORDER ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOCARDITIS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NIKOLSKY'S SIGN ( 2 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OSTEOPOROTIC FRACTURE ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PAIN OF SKIN ( 2 FDA reports)
PANCREATIC CARCINOMA ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHOTOPHOBIA ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMONIA ESCHERICHIA ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROSTATITIS ESCHERICHIA COLI ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
PULMONARY HYPERTENSION ( 2 FDA reports)
QUADRIPLEGIA ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RENAL CANCER METASTATIC ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
SIGMOIDITIS ( 2 FDA reports)
SINUS TACHYCARDIA ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THROMBOPHLEBITIS ( 2 FDA reports)
TONIC CLONIC MOVEMENTS ( 2 FDA reports)
TOOTH DISORDER ( 2 FDA reports)
TOOTH FRACTURE ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VISUAL FIELD DEFECT ( 2 FDA reports)
WITHDRAWAL SYNDROME ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL MASS ( 1 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACCOMMODATION DISORDER ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALLODYNIA ( 1 FDA reports)
AMMONIA ABNORMAL ( 1 FDA reports)
ANALGESIC DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANALGESIC DRUG LEVEL INCREASED ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANOREXIA NERVOSA ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APNOEA ( 1 FDA reports)
APPLICATION SITE HYPERSENSITIVITY ( 1 FDA reports)
APPLICATION SITE REACTION ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTERIOSPASM CORONARY ( 1 FDA reports)
ARTHRITIS BACTERIAL ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
AXONAL NEUROPATHY ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BILIARY DRAINAGE ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BLOOD CREATININE DECREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD OSMOLARITY INCREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BONE DISORDER ( 1 FDA reports)
BONE GRAFT ( 1 FDA reports)
BONE SWELLING ( 1 FDA reports)
BRAIN COMPRESSION ( 1 FDA reports)
BRAIN HERNIATION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BRONCHIAL FISTULA ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CATATONIA ( 1 FDA reports)
CENTRAL-ALVEOLAR HYPOVENTILATION ( 1 FDA reports)
CEREBELLAR ATAXIA ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL FOOT MALFORMATION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREPITATIONS ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
CYTOMEGALOVIRUS HEPATITIS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DISSOCIATIVE DISORDER ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DRUG ABUSER ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INTERACTION POTENTIATION ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSGLOBULINAEMIA ( 1 FDA reports)
EAR INFECTION FUNGAL ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ECZEMA IMPETIGINOUS ( 1 FDA reports)
EFFUSION ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
EMBOLISM VENOUS ( 1 FDA reports)
ENDODONTIC PROCEDURE ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
EYE DISORDER ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FINGER AMPUTATION ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
FOREIGN BODY ASPIRATION ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FULL BLOOD COUNT ABNORMAL ( 1 FDA reports)
FUNCTIONAL GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTRIC CANCER STAGE IV ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 1 FDA reports)
GENITAL HERPES ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
HAEMATOTOXICITY ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HAND AMPUTATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HIRSUTISM ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERCAPNIC ENCEPHALOPATHY ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTONIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOCAPNIA ( 1 FDA reports)
HYPOCHLORAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IMPLANT SITE REACTION ( 1 FDA reports)
IMPLANT SITE WARMTH ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INHIBITORY DRUG INTERACTION ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMATOMA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
KAPOSI'S SARCOMA ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LICHENOID KERATOSIS ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG TRANSPLANT ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTIC INFILTRATION ( 1 FDA reports)
MADAROSIS ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MENINGOMYELOCELE ( 1 FDA reports)
MENTAL RETARDATION ( 1 FDA reports)
METABOLIC ENCEPHALOPATHY ( 1 FDA reports)
METASTASES TO LYMPH NODES ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASES TO PLEURA ( 1 FDA reports)
METASTASES TO RETROPERITONEUM ( 1 FDA reports)
METASTASES TO SKIN ( 1 FDA reports)
METASTASES TO THE MEDIASTINUM ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
METASTATIC MALIGNANT MELANOMA ( 1 FDA reports)
METASTATIC RENAL CELL CARCINOMA ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NECROSIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROENDOCRINE CARCINOMA OF THE SKIN ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL CARCINOMA ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
OPTIC NEUROPATHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOLYSIS ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
PANCREATIC ENZYME ABNORMALITY ( 1 FDA reports)
PANCREATITIS CHRONIC ( 1 FDA reports)
PARAPLEGIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDITIS ( 1 FDA reports)
PERITONEAL EFFUSION ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHLEBOTHROMBOSIS ( 1 FDA reports)
PLEURITIC PAIN ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL HAEMATOMA ( 1 FDA reports)
PRIMARY SEQUESTRUM ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAL SEPSIS ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY NECROSIS ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MORBILLIFORM ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN GRAFT ( 1 FDA reports)
SKIN NODULE ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SKULL MALFORMATION ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
SUBCUTANEOUS ABSCESS ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUPERINFECTION ( 1 FDA reports)
SURGICAL PROCEDURE REPEATED ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THORACIC VERTEBRAL FRACTURE ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TOXIC NEUROPATHY ( 1 FDA reports)
TRANSMISSION OF DRUG VIA SEMEN ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
ULTRAFILTRATION FAILURE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE ENLARGEMENT ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VASCULAR DEMENTIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
VOLUME BLOOD DECREASED ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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