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

ASPARTATE AMINOTRANSFERASE INCREASED ( 32 FDA reports)
PNEUMONIA ( 29 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 26 FDA reports)
PAIN ( 26 FDA reports)
RENAL FAILURE ( 25 FDA reports)
PYREXIA ( 24 FDA reports)
BLOOD BILIRUBIN INCREASED ( 22 FDA reports)
MULTI-ORGAN FAILURE ( 21 FDA reports)
DEATH ( 19 FDA reports)
INJURY ( 19 FDA reports)
ANXIETY ( 18 FDA reports)
SEPTIC SHOCK ( 18 FDA reports)
RASH ( 17 FDA reports)
FEBRILE NEUTROPENIA ( 15 FDA reports)
MALAISE ( 14 FDA reports)
PLATELET COUNT DECREASED ( 14 FDA reports)
RESPIRATORY FAILURE ( 14 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 14 FDA reports)
BLOOD UREA INCREASED ( 13 FDA reports)
DIARRHOEA ( 13 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 12 FDA reports)
BLOOD CREATININE INCREASED ( 12 FDA reports)
LIVER DISORDER ( 12 FDA reports)
OEDEMA PERIPHERAL ( 12 FDA reports)
UNEVALUABLE EVENT ( 12 FDA reports)
ASTHENIA ( 11 FDA reports)
CARDIAC FAILURE ( 11 FDA reports)
CONDITION AGGRAVATED ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
HAEMODIALYSIS ( 11 FDA reports)
HEPATIC ENZYME INCREASED ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
HYPERKALAEMIA ( 10 FDA reports)
RENAL IMPAIRMENT ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
URINARY TRACT INFECTION ( 10 FDA reports)
WEIGHT DECREASED ( 10 FDA reports)
WEIGHT INCREASED ( 10 FDA reports)
ANAEMIA ( 9 FDA reports)
ANHEDONIA ( 9 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 9 FDA reports)
FALL ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
NAUSEA ( 9 FDA reports)
PANCYTOPENIA ( 9 FDA reports)
SHOCK ( 9 FDA reports)
STAPHYLOCOCCAL INFECTION ( 9 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 9 FDA reports)
VENOOCCLUSIVE LIVER DISEASE ( 9 FDA reports)
ANTITHROMBIN III DEFICIENCY ( 8 FDA reports)
BACK PAIN ( 8 FDA reports)
BLOOD POTASSIUM INCREASED ( 8 FDA reports)
DELIRIUM ( 8 FDA reports)
EMOTIONAL DISTRESS ( 8 FDA reports)
GRAFT VERSUS HOST DISEASE ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HYPOKALAEMIA ( 8 FDA reports)
INTERSTITIAL LUNG DISEASE ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
METABOLIC ACIDOSIS ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
TOXIC SKIN ERUPTION ( 8 FDA reports)
ANOREXIA ( 7 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 7 FDA reports)
ASCITES ( 7 FDA reports)
CONFUSIONAL STATE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
HEPATOCELLULAR INJURY ( 7 FDA reports)
PSEUDOMONAS INFECTION ( 7 FDA reports)
ATRIAL FIBRILLATION ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BONE MARROW FAILURE ( 6 FDA reports)
DEPRESSION ( 6 FDA reports)
EAR PAIN ( 6 FDA reports)
FEAR ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
HEART RATE IRREGULAR ( 6 FDA reports)
HEPATIC FAILURE ( 6 FDA reports)
HYPOMAGNESAEMIA ( 6 FDA reports)
LACTIC ACIDOSIS ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
NEUTROPENIA ( 6 FDA reports)
OSTEOARTHRITIS ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
PULMONARY CONGESTION ( 6 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 6 FDA reports)
RESPIRATORY ARREST ( 6 FDA reports)
RESPIRATORY DISORDER ( 6 FDA reports)
WALKING AID USER ( 6 FDA reports)
ABSCESS ORAL ( 5 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 5 FDA reports)
APLASTIC ANAEMIA ( 5 FDA reports)
BONE NEOPLASM MALIGNANT ( 5 FDA reports)
BURSITIS ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CELLULITIS ( 5 FDA reports)
CERVICAL NEURITIS ( 5 FDA reports)
CHILLS ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
DEAFNESS ( 5 FDA reports)
DECREASED INTEREST ( 5 FDA reports)
DISABILITY ( 5 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 5 FDA reports)
DUODENITIS ( 5 FDA reports)
DYSPHAGIA ( 5 FDA reports)
ESCHERICHIA SEPSIS ( 5 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 5 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 5 FDA reports)
HIATUS HERNIA ( 5 FDA reports)
HYDRONEPHROSIS ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOAESTHESIA FACIAL ( 5 FDA reports)
INFECTION ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
JOINT SPRAIN ( 5 FDA reports)
LUMBAR RADICULOPATHY ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
METASTASES TO LIVER ( 5 FDA reports)
MITRAL VALVE DISEASE ( 5 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 5 FDA reports)
MYALGIA ( 5 FDA reports)
MYELODYSPLASTIC SYNDROME ( 5 FDA reports)
MYELOPATHY ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NERVOUS SYSTEM DISORDER ( 5 FDA reports)
NEUROPATHY PERIPHERAL ( 5 FDA reports)
OSTEONECROSIS OF JAW ( 5 FDA reports)
OXYGEN SATURATION DECREASED ( 5 FDA reports)
PERIODONTITIS ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
RENAL CYST ( 5 FDA reports)
RENAL FAILURE CHRONIC ( 5 FDA reports)
RESPIRATORY DISTRESS ( 5 FDA reports)
RIB FRACTURE ( 5 FDA reports)
ROTATOR CUFF SYNDROME ( 5 FDA reports)
SCOLIOSIS ( 5 FDA reports)
SINUS HEADACHE ( 5 FDA reports)
SINUSITIS ( 5 FDA reports)
SOMNOLENCE ( 5 FDA reports)
SPINAL COLUMN STENOSIS ( 5 FDA reports)
SPINAL COMPRESSION FRACTURE ( 5 FDA reports)
SUDDEN DEATH ( 5 FDA reports)
TOOTHACHE ( 5 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 5 FDA reports)
TRIGEMINAL NEURALGIA ( 5 FDA reports)
ABDOMINAL DISTENSION ( 4 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 4 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
BLOOD CREATINE INCREASED ( 4 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 4 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
COAGULOPATHY ( 4 FDA reports)
COUGH ( 4 FDA reports)
CYTOLYTIC HEPATITIS ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
FLUID OVERLOAD ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 4 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
NEUTROPHIL COUNT DECREASED ( 4 FDA reports)
PETECHIAE ( 4 FDA reports)
PNEUMONIA FUNGAL ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH MACULO-PAPULAR ( 4 FDA reports)
RESPIRATION ABNORMAL ( 4 FDA reports)
RHABDOMYOLYSIS ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SLEEP PHASE RHYTHM DISTURBANCE ( 4 FDA reports)
SUICIDAL IDEATION ( 4 FDA reports)
TORSADE DE POINTES ( 4 FDA reports)
UROSEPSIS ( 4 FDA reports)
VENTRICULAR FIBRILLATION ( 4 FDA reports)
ABNORMAL BEHAVIOUR ( 3 FDA reports)
ABULIA ( 3 FDA reports)
AGRANULOCYTOSIS ( 3 FDA reports)
AORTIC INJURY ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD CORTISOL INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BONE MARROW DEPRESSION ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
CARDIOMEGALY ( 3 FDA reports)
CARNITINE DEFICIENCY ( 3 FDA reports)
CERUMEN IMPACTION ( 3 FDA reports)
CERVICAL SPINAL STENOSIS ( 3 FDA reports)
CHOLELITHIASIS ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLITIS ISCHAEMIC ( 3 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 3 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 3 FDA reports)
DECREASED ACTIVITY ( 3 FDA reports)
DECREASED APPETITE ( 3 FDA reports)
DERMATITIS BULLOUS ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DYSKINESIA ( 3 FDA reports)
ENDODONTIC PROCEDURE ( 3 FDA reports)
ENGRAFT FAILURE ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HEPATITIS B ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
INTESTINAL PERFORATION ( 3 FDA reports)
KIDNEY INFECTION ( 3 FDA reports)
LETHARGY ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
MENTAL DISORDER ( 3 FDA reports)
NASAL CONGESTION ( 3 FDA reports)
NASAL SEPTUM DEVIATION ( 3 FDA reports)
NEOPLASM MALIGNANT ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 3 FDA reports)
POLYNEUROPATHY ( 3 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
SEQUESTRECTOMY ( 3 FDA reports)
SICKLE CELL ANAEMIA WITH CRISIS ( 3 FDA reports)
STRESS ( 3 FDA reports)
SYNCOPE VASOVAGAL ( 3 FDA reports)
THROAT TIGHTNESS ( 3 FDA reports)
TOOTH EXTRACTION ( 3 FDA reports)
TRACHEO-OESOPHAGEAL FISTULA ( 3 FDA reports)
TRICHOSPORON INFECTION ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VESICAL FISTULA ( 3 FDA reports)
VOMITING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
APNOEA ( 2 FDA reports)
BARRETT'S OESOPHAGUS ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLUNTED AFFECT ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BRAIN STEM HAEMORRHAGE ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPLICATIONS OF TRANSPLANTED KIDNEY ( 2 FDA reports)
CONJUNCTIVAL DISORDER ( 2 FDA reports)
CRYPTOGENIC ORGANISING PNEUMONIA ( 2 FDA reports)
CYSTITIS HAEMORRHAGIC ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIVERTICULUM ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
GASTRITIS ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GRAFT VERSUS HOST DISEASE IN LUNG ( 2 FDA reports)
HAEMANGIOMA ( 2 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
HYPOPHOSPHATAEMIA ( 2 FDA reports)
HYPOTHERMIA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
MEDIASTINITIS ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MIXED LIVER INJURY ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MUCOUS MEMBRANE DISORDER ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROTOXICITY ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
OSTEOLYSIS ( 2 FDA reports)
PERIPHERAL SENSORY NEUROPATHY ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RALES ( 2 FDA reports)
REYE'S SYNDROME ( 2 FDA reports)
SEPSIS SYNDROME ( 2 FDA reports)
SEPTIC EMBOLUS ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
STENOTROPHOMONAS INFECTION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SYSTEMIC CANDIDA ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TINNITUS ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL INFECTION ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
ACUTE MYELOID LEUKAEMIA RECURRENT ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIOPATHY ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APPETITE DISORDER ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIAL TEST POSITIVE ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BED REST ( 1 FDA reports)
BICYTOPENIA ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN UNCONJUGATED INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIOACTIVE DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARNITINE DECREASED ( 1 FDA reports)
CAROTID BRUIT ( 1 FDA reports)
CATHETER CULTURE POSITIVE ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM INFECTION ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ACUTE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 1 FDA reports)
COAGULATION FACTOR V LEVEL DECREASED ( 1 FDA reports)
COAGULATION FACTOR V LEVEL INCREASED ( 1 FDA reports)
CONDUCTION DISORDER ( 1 FDA reports)
CONGENITAL ANOMALY ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
CREATININE RENAL CLEARANCE INCREASED ( 1 FDA reports)
CYTOMEGALOVIRUS TEST POSITIVE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALITIS CYTOMEGALOVIRUS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESSENTIAL HYPERTENSION ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
FEAR OF DEATH ( 1 FDA reports)
FEBRILE BONE MARROW APLASIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GALLBLADDER INJURY ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL SOUNDS ABNORMAL ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOCHROMATOSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 1 FDA reports)
HAEMOSIDEROSIS ( 1 FDA reports)
HAEMOSTASIS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATIC ISCHAEMIA ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGAMMAGLOBULINAEMIA BENIGN MONOCLONAL ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOPNOEA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCORRECT STORAGE OF DRUG ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFECTIVE SPONDYLITIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE ERYTHEMA ( 1 FDA reports)
INFUSION SITE RASH ( 1 FDA reports)
INFUSION SITE WARMTH ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRAVASCULAR HAEMOLYSIS ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
LABILE HYPERTENSION ( 1 FDA reports)
LARGE GRANULAR LYMPHOCYTOSIS ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LIP DISORDER ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LUMBAR SPINAL STENOSIS ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MEAN CELL VOLUME INCREASED ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
MITRAL VALVE CALCIFICATION ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE INJURIES ( 1 FDA reports)
MULTIPLE-DRUG RESISTANCE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCLONUS ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PERIRECTAL ABSCESS ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
PNEUMONIA BACTERIAL ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSYCHOLOGICAL TRAUMA ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PUPIL FIXED ( 1 FDA reports)
PURPURA ( 1 FDA reports)
PUS IN STOOL ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RECTAL CANCER ( 1 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL TUBULAR NECROSIS ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
SCAB ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
SHOCK HAEMORRHAGIC ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPLEEN DISORDER ( 1 FDA reports)
SPLENIC LESION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL ABSCESS ( 1 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STEM CELL TRANSPLANT ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
THERAPEUTIC PRODUCT INEFFECTIVE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TYPE 2 DIABETES MELLITUS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 1 FDA reports)
VENOUS THROMBOSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VOCAL CORD PARALYSIS ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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