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DEPRESSED LEVEL OF CONSCIOUSNESS ( 20 FDA reports)
HALLUCINATION ( 15 FDA reports)
FALL ( 13 FDA reports)
HYPOGLYCAEMIA ( 13 FDA reports)
PYREXIA ( 12 FDA reports)
TREMOR ( 12 FDA reports)
DIARRHOEA ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
DYSARTHRIA ( 10 FDA reports)
PNEUMONIA ( 10 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 9 FDA reports)
LIVER DISORDER ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
HYPONATRAEMIA ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
JAUNDICE ( 8 FDA reports)
OEDEMA PERIPHERAL ( 8 FDA reports)
RENAL IMPAIRMENT ( 8 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
DELIRIUM ( 7 FDA reports)
DYSPHAGIA ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
DELUSION ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 6 FDA reports)
HYPERGLYCAEMIA ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
MOVEMENT DISORDER ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
SOMNOLENCE ( 6 FDA reports)
VOMITING ( 6 FDA reports)
BLADDER CANCER ( 5 FDA reports)
BLOOD ANTIDIURETIC HORMONE INCREASED ( 5 FDA reports)
BLOOD OSMOLARITY DECREASED ( 5 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 5 FDA reports)
CONVULSION ( 5 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 5 FDA reports)
INTESTINAL OBSTRUCTION ( 5 FDA reports)
MUSCULOSKELETAL PAIN ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PLEURAL EFFUSION ( 5 FDA reports)
RENAL DISORDER ( 5 FDA reports)
RESTLESSNESS ( 5 FDA reports)
ROAD TRAFFIC ACCIDENT ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
VITH NERVE PARALYSIS ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ANOREXIA ( 4 FDA reports)
ATELECTASIS ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
ATRIOVENTRICULAR BLOCK ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 4 FDA reports)
BRADYCARDIA ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIZZINESS ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
ILEUS ( 4 FDA reports)
METABOLIC ACIDOSIS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
SMALL INTESTINE CARCINOMA ( 4 FDA reports)
URINE OSMOLARITY INCREASED ( 4 FDA reports)
ABASIA ( 3 FDA reports)
AGGRESSION ( 3 FDA reports)
ANAEMIA ( 3 FDA reports)
ASTHMA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CAROTID ARTERY STENOSIS ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
GENERALISED OEDEMA ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HELICOBACTER TEST POSITIVE ( 3 FDA reports)
HEPATITIS FULMINANT ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LYMPHOMA ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
PANCYTOPENIA ( 3 FDA reports)
PETECHIAE ( 3 FDA reports)
PORIOMANIA ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PSYCHIATRIC SYMPTOM ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
RENAL ARTERY STENOSIS ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
SENSORY DISTURBANCE ( 3 FDA reports)
SINUS ARREST ( 3 FDA reports)
SUDDEN ONSET OF SLEEP ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
VOLVULUS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 2 FDA reports)
ANAPHYLACTOID REACTION ( 2 FDA reports)
ANGER ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMA HEPATIC ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DIABETIC KETOACIDOSIS ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EPULIS ( 2 FDA reports)
EXTRAOCULAR MUSCLE PARESIS ( 2 FDA reports)
FACIAL PARESIS ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEMORAL NECK FRACTURE ( 2 FDA reports)
FOOT FRACTURE ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GLOSSOPTOSIS ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC CYST ( 2 FDA reports)
HEPATIC ENCEPHALOPATHY ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTONIA ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LEG AMPUTATION ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
METABOLIC ALKALOSIS ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
ORAL HERPES ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PHRENIC NERVE PARALYSIS ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RETINAL OEDEMA ( 2 FDA reports)
RIB FRACTURE ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH MASS ( 2 FDA reports)
SUICIDE ATTEMPT ( 2 FDA reports)
TAKAYASU'S ARTERITIS ( 2 FDA reports)
THIRST ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TUMOUR LYSIS SYNDROME ( 2 FDA reports)
UNRESPONSIVE TO STIMULI ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
ABDOMEN CRUSHING ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ALVEOLITIS ALLERGIC ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODY POSITIVE VASCULITIS ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
COMMUNICATION DISORDER ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CYSTITIS HAEMORRHAGIC ( 1 FDA reports)
DEVICE DISLOCATION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ACUTE ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HELICOBACTER INFECTION ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOPROTEINAEMIA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL POLYP HAEMORRHAGE ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LIMB CRUSHING INJURY ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METAMORPHOPSIA ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NYSTAGMUS ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL ULCER ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
PULMONARY FIBROSIS ( 1 FDA reports)
REFLUX OESOPHAGITIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SOLILOQUY ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPLENIC NEOPLASM MALIGNANCY UNSPECIFIED ( 1 FDA reports)
SPLENOMEGALY ( 1 FDA reports)
T-CELL LYMPHOMA ( 1 FDA reports)
THYROID ADENOMA ( 1 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VERBAL ABUSE ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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