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

DYSPNOEA ( 26 FDA reports)
VOMITING ( 18 FDA reports)
PYREXIA ( 15 FDA reports)
NAUSEA ( 14 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
DIZZINESS ( 11 FDA reports)
MYOCARDIAL INFARCTION ( 11 FDA reports)
ASTHENIA ( 10 FDA reports)
CHEST PAIN ( 10 FDA reports)
COUGH ( 10 FDA reports)
DIARRHOEA ( 10 FDA reports)
DRUG INTERACTION ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
RESPIRATORY FAILURE ( 10 FDA reports)
SEPSIS ( 10 FDA reports)
ASTHMA ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
RENAL FAILURE ACUTE ( 9 FDA reports)
WEIGHT DECREASED ( 9 FDA reports)
BLOOD AMYLASE INCREASED ( 8 FDA reports)
CHOLELITHIASIS ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
PNEUMONIA ( 8 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 7 FDA reports)
ANAEMIA ( 7 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 7 FDA reports)
HYPERHIDROSIS ( 7 FDA reports)
MESOTHELIOMA ( 7 FDA reports)
RASH ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
URTICARIA ( 7 FDA reports)
ARTHRALGIA ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
COMA ( 6 FDA reports)
CONFUSIONAL STATE ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 6 FDA reports)
EMPHYSEMA ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
MALAISE ( 6 FDA reports)
METABOLIC ACIDOSIS ( 6 FDA reports)
PAIN ( 6 FDA reports)
RENAL IMPAIRMENT ( 6 FDA reports)
TREMOR ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ABDOMINAL PAIN ( 5 FDA reports)
APHASIA ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CHILLS ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
FALL ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HAEMODIALYSIS ( 5 FDA reports)
HALLUCINATION, VISUAL ( 5 FDA reports)
HYPERTENSION ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
HYPOTENSION ( 5 FDA reports)
OEDEMA PERIPHERAL ( 5 FDA reports)
OESOPHAGEAL ULCER ( 5 FDA reports)
PARANOIA ( 5 FDA reports)
PULMONARY EMBOLISM ( 5 FDA reports)
REFLUX OESOPHAGITIS ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
AGITATION ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ASCITES ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BLOOD CORTISOL DECREASED ( 4 FDA reports)
BLOOD UREA INCREASED ( 4 FDA reports)
BONE PAIN ( 4 FDA reports)
BURNING SENSATION ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
COLD SWEAT ( 4 FDA reports)
DECREASED APPETITE ( 4 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 4 FDA reports)
DRUG TOXICITY ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
KLEBSIELLA INFECTION ( 4 FDA reports)
LEFT VENTRICULAR FAILURE ( 4 FDA reports)
LUNG NEOPLASM MALIGNANT ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
NEUTROPENIA ( 4 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
APNOEA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CHLORIDE DECREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
BRONCHIECTASIS ( 3 FDA reports)
BRONCHOPNEUMONIA ( 3 FDA reports)
CARDIAC FAILURE ( 3 FDA reports)
CATHETER SITE INFECTION ( 3 FDA reports)
CLOSTRIDIUM COLITIS ( 3 FDA reports)
CORONARY ARTERY OCCLUSION ( 3 FDA reports)
CUSHING'S SYNDROME ( 3 FDA reports)
DEATH ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
HEPATORENAL SYNDROME ( 3 FDA reports)
HYPOKALAEMIA ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 3 FDA reports)
MELAENA ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MULTI-ORGAN FAILURE ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
PNEUMOTHORAX ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
PREGNANCY ( 3 FDA reports)
PROCEDURAL COMPLICATION ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PSYCHOTIC DISORDER ( 3 FDA reports)
RALES ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY RATE INCREASED ( 3 FDA reports)
RESUSCITATION ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TACHYPNOEA ( 3 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ADENOVIRUS INFECTION ( 2 FDA reports)
ADRENAL SUPPRESSION ( 2 FDA reports)
ADRENOCORTICAL INSUFFICIENCY ACUTE ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ANURIA ( 2 FDA reports)
AORTIC DISSECTION ( 2 FDA reports)
APLASTIC ANAEMIA ( 2 FDA reports)
APPLICATION SITE DERMATITIS ( 2 FDA reports)
APPLICATION SITE ERYTHEMA ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLOOD CORTICOTROPHIN ( 2 FDA reports)
BLOOD CORTICOTROPHIN ABNORMAL ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD PH DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
CAESAREAN SECTION ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CARDIAC FLUTTER ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CHEST X-RAY ABNORMAL ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISTURBANCE IN ATTENTION ( 2 FDA reports)
DRUG EFFECT INCREASED ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
EUPHORIC MOOD ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATIC FAILURE ( 2 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 2 FDA reports)
INJECTION SITE ERYTHEMA ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG HYPERINFLATION ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALIGNANT URINARY TRACT NEOPLASM ( 2 FDA reports)
MENTAL IMPAIRMENT ( 2 FDA reports)
MONOPARESIS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NEUTROPENIC SEPSIS ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OVERDOSE ( 2 FDA reports)
OVERWEIGHT ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PALPITATIONS ( 2 FDA reports)
PARESIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PETIT MAL EPILEPSY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PHLEBOTHROMBOSIS ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
PURPURA ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
RESPIRATION ABNORMAL ( 2 FDA reports)
RESPIRATORY DEPRESSION ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RHONCHI ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TRACHEOSTOMY ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL OBESITY ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABDOMINAL WALL DISORDER ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE PRERENAL FAILURE ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGLE CLOSURE GLAUCOMA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL DECREASED ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARNOLD-CHIARI MALFORMATION ( 1 FDA reports)
ARTERIAL SPASM ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATHEROSCLEROSIS ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BARRETT'S OESOPHAGUS ( 1 FDA reports)
BASE EXCESS INCREASED ( 1 FDA reports)
BENIGN NEOPLASM OF SKIN ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES ABNORMAL ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BOVINE TUBERCULOSIS ( 1 FDA reports)
BOWEL SOUNDS ABNORMAL ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHIAL OBSTRUCTION ( 1 FDA reports)
BRONCHOALVEOLAR LAVAGE ABNORMAL ( 1 FDA reports)
CAMPYLOBACTER INFECTION ( 1 FDA reports)
CARDIAC MONITORING ABNORMAL ( 1 FDA reports)
CARDIAC OUTPUT DECREASED ( 1 FDA reports)
CARDIAC STRESS TEST ABNORMAL ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CATHETER SEPSIS ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLESTASIS ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
CONCUSSION ( 1 FDA reports)
CONDUCTIVE DEAFNESS ( 1 FDA reports)
CONGENITAL PULMONARY ARTERY ANOMALY ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTRAST MEDIA REACTION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CRYPTOGENIC ORGANIZING PNEUMONIA ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELUSIONAL DISORDER, PERSECUTORY TYPE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEPRESSION SUICIDAL ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISTURBANCE IN SOCIAL BEHAVIOUR ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DEPENDENCE ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG LEVEL FLUCTUATING ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHASIA ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR CONGESTION ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ECHOCARDIOGRAM ABNORMAL ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM QT CORRECTED INTERVAL PROLONGED ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
ENURESIS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ERYTHEMA INFECTIOSUM ( 1 FDA reports)
EXCITABILITY ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
FEAR ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FURUNCLE ( 1 FDA reports)
GASTRIC OPERATION ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GASTROINTESTINAL CANCER METASTATIC ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENITAL BURNING SENSATION ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GRAFT DYSFUNCTION ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT INCREASED ( 1 FDA reports)
HAEMOGLOBIN INCREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 1 FDA reports)
HAEMOTHORAX ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HAPTOGLOBIN DECREASED ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS TOXIC ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYDRONEPHROSIS ( 1 FDA reports)
HYDROXYCORTICOSTEROIDS INCREASED ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCAPNIA ( 1 FDA reports)
HYPERCHLORAEMIA ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
IMPRISONMENT ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INDURATION ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTRA-ABDOMINAL HAEMORRHAGE ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
INTRACRANIAL PRESSURE INCREASED ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
IRIDOCELE ( 1 FDA reports)
IRIS HAEMORRHAGE ( 1 FDA reports)
IRON DEFICIENCY ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACTIC ACIDOSIS ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LUNG CREPITATION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
METABOLIC ALKALOSIS ( 1 FDA reports)
METRORRHAGIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MONOCYTE COUNT DECREASED ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE FRACTURES ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROPATHY TOXIC ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER METASTATIC ( 1 FDA reports)
OESOPHAGEAL OEDEMA ( 1 FDA reports)
OPTIC NERVE CUPPING ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORBITAL OEDEMA ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PCO2 INCREASED ( 1 FDA reports)
PELVIC HAEMATOMA ( 1 FDA reports)
PERIORBITAL HAEMATOMA ( 1 FDA reports)
PERIPHERAL COLDNESS ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURAL FIBROSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA LEGIONELLA ( 1 FDA reports)
PNEUMONITIS ( 1 FDA reports)
POLYCYTHAEMIA ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEINURIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PUBIC RAMI FRACTURE ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY EOSINOPHILIA ( 1 FDA reports)
PULMONARY MALFORMATION ( 1 FDA reports)
PULMONARY TOXICITY ( 1 FDA reports)
PULMONARY TUBERCULOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
PURPURA FULMINANS ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REACTION TO MEDICAL AGENT PRESERVATIVES ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL ONCOCYTOMA ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETICULOCYTE COUNT INCREASED ( 1 FDA reports)
RETROPERITONEAL HAEMATOMA ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SENSORY LOSS ( 1 FDA reports)
SERRATIA INFECTION ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP WALKING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINA BIFIDA ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STATUS ASTHMATICUS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STRESS ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBILEUS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
SYNOVITIS ( 1 FDA reports)
TACHYCARDIA PAROXYSMAL ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
TROPONIN I INCREASED ( 1 FDA reports)
TROPONIN INCREASED ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
ULTRASOUND KIDNEY ABNORMAL ( 1 FDA reports)
UNINTENDED PREGNANCY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETHRAL MEATUS STENOSIS ( 1 FDA reports)
URINE ANALYSIS ABNORMAL ( 1 FDA reports)
VASCULAR OCCLUSION ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VIRAL RASH ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)

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