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

DRUG INTERACTION ( 38 FDA reports)
PNEUMONIA ( 37 FDA reports)
PYREXIA ( 34 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 30 FDA reports)
JAUNDICE ( 25 FDA reports)
CONVULSION ( 24 FDA reports)
DYSPNOEA ( 23 FDA reports)
DIARRHOEA ( 22 FDA reports)
ANAPHYLACTIC REACTION ( 21 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 21 FDA reports)
LIVE BIRTH ( 21 FDA reports)
CHOLESTASIS OF PREGNANCY ( 19 FDA reports)
VOMITING ( 18 FDA reports)
HYPERSENSITIVITY ( 17 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 17 FDA reports)
DIZZINESS ( 16 FDA reports)
NAUSEA ( 16 FDA reports)
PLEURAL EFFUSION ( 15 FDA reports)
PREMATURE LABOUR ( 15 FDA reports)
TACHYCARDIA ( 15 FDA reports)
HEADACHE ( 14 FDA reports)
MYOPATHY ( 14 FDA reports)
SEPSIS ( 14 FDA reports)
CARDIAC FAILURE ( 13 FDA reports)
CEREBRAL HAEMORRHAGE ( 13 FDA reports)
RENAL FAILURE ACUTE ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
RESPIRATORY FAILURE ( 13 FDA reports)
SUBDURAL HAEMORRHAGE ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
ANAEMIA ( 11 FDA reports)
DEHYDRATION ( 11 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 11 FDA reports)
DRUG LEVEL DECREASED ( 11 FDA reports)
HAEMORRHAGE ( 11 FDA reports)
RASH ( 11 FDA reports)
STEVENS-JOHNSON SYNDROME ( 11 FDA reports)
CARDIAC ARREST ( 10 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 10 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 10 FDA reports)
HYPERCALCAEMIA ( 10 FDA reports)
HYPOTENSION ( 10 FDA reports)
MYOCARDIAL INFARCTION ( 10 FDA reports)
OEDEMA PERIPHERAL ( 10 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 10 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
DECREASED APPETITE ( 9 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 9 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 9 FDA reports)
URTICARIA ( 9 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
ERYTHEMA ( 8 FDA reports)
HYPOXIA ( 8 FDA reports)
MALAISE ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
PAIN ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
SEPTIC SHOCK ( 8 FDA reports)
SOMNOLENCE ( 8 FDA reports)
VIITH NERVE PARALYSIS ( 8 FDA reports)
ARRHYTHMIA ( 7 FDA reports)
ATRIAL SEPTAL DEFECT ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
BLOOD PRESSURE DECREASED ( 7 FDA reports)
BONE DISORDER ( 7 FDA reports)
CEREBRAL INFARCTION ( 7 FDA reports)
CHOLESTASIS ( 7 FDA reports)
DRUG INEFFECTIVE ( 7 FDA reports)
HYPERTENSION ( 7 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 7 FDA reports)
MUSCULAR WEAKNESS ( 7 FDA reports)
ORAL DISORDER ( 7 FDA reports)
ORAL HERPES ( 7 FDA reports)
PAIN IN JAW ( 7 FDA reports)
PREMATURE BABY ( 7 FDA reports)
THROMBOCYTOPENIA ( 7 FDA reports)
TOOTH EXTRACTION ( 7 FDA reports)
TREMOR ( 7 FDA reports)
URINARY TRACT INFECTION ( 7 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
AGRANULOCYTOSIS ( 6 FDA reports)
ANHEDONIA ( 6 FDA reports)
ANXIETY ( 6 FDA reports)
ARTERIOSCLEROSIS ( 6 FDA reports)
ASBESTOSIS ( 6 FDA reports)
BACTERIAL INFECTION ( 6 FDA reports)
BONE DENSITY DECREASED ( 6 FDA reports)
BONE PAIN ( 6 FDA reports)
BRAIN OEDEMA ( 6 FDA reports)
BREAKTHROUGH PAIN ( 6 FDA reports)
BRONCHOSPASM ( 6 FDA reports)
CHEST TUBE INSERTION ( 6 FDA reports)
CHOLECYSTECTOMY ( 6 FDA reports)
CHOLECYSTITIS INFECTIVE ( 6 FDA reports)
DENTURE WEARER ( 6 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 6 FDA reports)
EXCORIATION ( 6 FDA reports)
GINGIVAL DISORDER ( 6 FDA reports)
GINGIVAL OEDEMA ( 6 FDA reports)
HAEMARTHROSIS ( 6 FDA reports)
HIP FRACTURE ( 6 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 6 FDA reports)
IMPAIRED HEALING ( 6 FDA reports)
INJURY ( 6 FDA reports)
JAW DISORDER ( 6 FDA reports)
LOOSE TOOTH ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
MENTAL STATUS CHANGES ( 6 FDA reports)
METASTASES TO BONE ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
OXYGEN SATURATION DECREASED ( 6 FDA reports)
PANCYTOPENIA ( 6 FDA reports)
PLEURAL DECORTICATION ( 6 FDA reports)
PREGNANCY ( 6 FDA reports)
PROSTATE CANCER METASTATIC ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
TOOTH DISORDER ( 6 FDA reports)
TOOTH LOSS ( 6 FDA reports)
TRANSFUSION ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ABDOMINAL DISTENSION ( 5 FDA reports)
ANAPHYLACTIC SHOCK ( 5 FDA reports)
ASCITES ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BILIARY SEPSIS ( 5 FDA reports)
BLOOD PRESSURE INCREASED ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DEATH ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 5 FDA reports)
HAEMOGLOBIN DECREASED ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HEPATOCELLULAR INJURY ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
JAUNDICE CHOLESTATIC ( 5 FDA reports)
LIVER INJURY ( 5 FDA reports)
LYMPHADENOPATHY ( 5 FDA reports)
MALLORY-WEISS SYNDROME ( 5 FDA reports)
RASH MACULO-PAPULAR ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SUICIDAL IDEATION ( 5 FDA reports)
THORACOSTOMY ( 5 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 5 FDA reports)
VENTRICULAR FIBRILLATION ( 5 FDA reports)
ABDOMINAL HERNIA ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
BLOOD ALBUMIN INCREASED ( 4 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARDIO-RESPIRATORY ARREST ( 4 FDA reports)
CEREBRAL ARTERIOSCLEROSIS ( 4 FDA reports)
CHOLELITHIASIS ( 4 FDA reports)
CIRCULATORY COLLAPSE ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
ERYSIPELAS ( 4 FDA reports)
FIBRINOLYSIS ( 4 FDA reports)
GRANULOCYTOPENIA ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HEPATIC FAILURE ( 4 FDA reports)
HEPATIC FIBROSIS ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
INDUCED LABOUR ( 4 FDA reports)
INFECTION ( 4 FDA reports)
JAW OPERATION ( 4 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 4 FDA reports)
LYMPHOCELE ( 4 FDA reports)
NEUROMYOPATHY ( 4 FDA reports)
NEUTROPENIC SEPSIS ( 4 FDA reports)
OSTEONECROSIS ( 4 FDA reports)
OSTEONECROSIS OF JAW ( 4 FDA reports)
PHOTOSENSITIVITY REACTION ( 4 FDA reports)
PLATELET COUNT DECREASED ( 4 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 4 FDA reports)
POST PROCEDURAL COMPLICATION ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RASH PUSTULAR ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
SCAR ( 4 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ANOREXIA ( 3 FDA reports)
ANTIBIOTIC LEVEL BELOW THERAPEUTIC ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD LACTATE DEHYDROGENASE DECREASED ( 3 FDA reports)
BRONCHITIS ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CEREBELLAR ATROPHY ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
COUGH ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DEPRESSION ( 3 FDA reports)
DERMATITIS EXFOLIATIVE ( 3 FDA reports)
DEVICE RELATED INFECTION ( 3 FDA reports)
DILATATION VENTRICULAR ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 3 FDA reports)
EOSINOPHILIA ( 3 FDA reports)
EPILEPSY ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FALL ( 3 FDA reports)
GASTROENTERITIS ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
GINGIVAL BLEEDING ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HIP SURGERY ( 3 FDA reports)
HYPERKALAEMIA ( 3 FDA reports)
INCISION SITE COMPLICATION ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INTERSTITIAL LUNG DISEASE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG INFECTION ( 3 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
NEUTROPENIA ( 3 FDA reports)
OCULAR HYPERAEMIA ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
OPEN REDUCTION OF FRACTURE ( 3 FDA reports)
OSTEOPENIA ( 3 FDA reports)
PNEUMONIA ASPIRATION ( 3 FDA reports)
PSOAS ABSCESS ( 3 FDA reports)
RASH GENERALISED ( 3 FDA reports)
SERUM FERRITIN INCREASED ( 3 FDA reports)
SHOCK ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SUBILEUS ( 3 FDA reports)
TARDIVE DYSKINESIA ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
TONGUE DISCOLOURATION ( 3 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
URINE OUTPUT DECREASED ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WOUND DEHISCENCE ( 3 FDA reports)
WOUND INFECTION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ABSCESS ( 2 FDA reports)
ACCIDENTAL DEATH ( 2 FDA reports)
ACCIDENTAL OVERDOSE ( 2 FDA reports)
ACUTE ABDOMEN ( 2 FDA reports)
ACUTE CORONARY SYNDROME ( 2 FDA reports)
AEROMONA INFECTION ( 2 FDA reports)
ALVEOLITIS ALLERGIC ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
ANTIDIURETIC HORMONE ABNORMALITY ( 2 FDA reports)
AORTIC ARTERIOSCLEROSIS ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASPIRATION PLEURAL CAVITY ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BETA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 2 FDA reports)
BILE DUCT OBSTRUCTION ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD ELECTROLYTES INCREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
BRONCHOPNEUMONIA ( 2 FDA reports)
CHILLS ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CLOSTRIDIUM DIFFICILE COLITIS ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COMA ( 2 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
ENDOCARDITIS STAPHYLOCOCCAL ( 2 FDA reports)
ENTERITIS ( 2 FDA reports)
ENTEROCOCCAL INFECTION ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
EPSTEIN-BARR VIRUS ANTIGEN POSITIVE ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FEAR ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEEDING DISORDER ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FIBRIN D DIMER DECREASED ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
GRANULOCYTE COUNT DECREASED ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATIC ENZYME ABNORMAL ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATOMEGALY ( 2 FDA reports)
HEPATOTOXICITY ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERPYREXIA ( 2 FDA reports)
HYPERVOLAEMIA ( 2 FDA reports)
HYPONATRAEMIA ( 2 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 2 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 2 FDA reports)
INCISION SITE HAEMORRHAGE ( 2 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 2 FDA reports)
INJECTION SITE HAEMORRHAGE ( 2 FDA reports)
INTESTINAL PROLAPSE ( 2 FDA reports)
LARYNGITIS ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LINEAR IGA DISEASE ( 2 FDA reports)
LOBAR PNEUMONIA ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MENORRHAGIA ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
MOTOR DEVELOPMENTAL DELAY ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEUROLEPTIC MALIGNANT SYNDROME ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NYSTAGMUS ( 2 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 2 FDA reports)
ORGANISING PNEUMONIA ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PERICARDIAL DRAINAGE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERITONEAL DIALYSIS ( 2 FDA reports)
PERITONITIS ( 2 FDA reports)
PERSECUTORY DELUSION ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMOMEDIASTINUM ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMONIA KLEBSIELLA ( 2 FDA reports)
POLYSEROSITIS ( 2 FDA reports)
POST PROCEDURAL URINE LEAK ( 2 FDA reports)
POST THROMBOTIC SYNDROME ( 2 FDA reports)
PREGNANCY ON ORAL CONTRACEPTIVE ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RENAL ARTERY STENOSIS ( 2 FDA reports)
RENAL DISORDER ( 2 FDA reports)
RESPIRATORY DISTRESS ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SUBCUTANEOUS HAEMATOMA ( 2 FDA reports)
SUTURE RUPTURE ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWELLING FACE ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TACHYPNOEA ( 2 FDA reports)
THERMAL BURN ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TRICHOSPORON INFECTION ( 2 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 2 FDA reports)
TUBERCULOSIS ( 2 FDA reports)
ULCER ( 2 FDA reports)
URETERIC STENOSIS ( 2 FDA reports)
VISUAL DISTURBANCE ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE TONSILLITIS ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAL DILATATION ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGINA UNSTABLE ( 1 FDA reports)
ANTICOAGULATION DRUG LEVEL ABOVE THERAPEUTIC ( 1 FDA reports)
ANTIMICROBIAL SUSCEPTIBILITY TEST RESISTANT ( 1 FDA reports)
AORTIC THROMBOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
B-LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
BILE DUCT STENOSIS ( 1 FDA reports)
BILEVEL POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRONCHOPLEURAL FISTULA ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ALCOHOLIC ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CERUMEN IMPACTION ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST ( 1 FDA reports)
CLOSTRIDIUM DIFFICILE TOXIN TEST POSITIVE ( 1 FDA reports)
CLOSTRIDIUM TEST POSITIVE ( 1 FDA reports)
CONTINUOUS POSITIVE AIRWAY PRESSURE ( 1 FDA reports)
CRYPTOSPORIDIOSIS INFECTION ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIET REFUSAL ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DIVERTICULAR PERFORATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SPECIFIC ANTIBODY PRESENT ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROMECHANICAL DISSOCIATION ( 1 FDA reports)
EMPYEMA ( 1 FDA reports)
ENTERITIS NECROTICANS ( 1 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 1 FDA reports)
EVACUATION OF RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXTRAVASATION BLOOD ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBRIN DECREASED ( 1 FDA reports)
FLUID INTAKE REDUCED ( 1 FDA reports)
FLUID OVERLOAD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
FRACTURED SACRUM ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC CEREBRAL INFARCTION ( 1 FDA reports)
HAEMORRHAGIC DIATHESIS ( 1 FDA reports)
HALLUCINATION, VISUAL ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENCEPHALOPATHY ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC INFARCTION ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPLASTIC LEFT HEART SYNDROME ( 1 FDA reports)
HYPOXIC ENCEPHALOPATHY ( 1 FDA reports)
IDEAS OF REFERENCE ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 1 FDA reports)
INFECTIOUS MONONUCLEOSIS ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTION TREMOR ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
KOUNIS SYNDROME ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LABOUR INDUCTION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LARYNGOSPASM ( 1 FDA reports)
LONG QT SYNDROME ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARROW HYPERPLASIA ( 1 FDA reports)
MASTOIDITIS ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METHICILLIN-RESISTANT STAPHYLOCOCCAL AUREUS TEST POSITIVE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MITRAL VALVE REPLACEMENT ( 1 FDA reports)
MORAXELLA INFECTION ( 1 FDA reports)
MUCOSAL HAEMORRHAGE ( 1 FDA reports)
MUCOSAL ULCERATION ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
MUSCLE CONTRACTIONS INVOLUNTARY ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NARCOTIC INTOXICATION ( 1 FDA reports)
NEONATAL ASPIRATION ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OPERATIVE HAEMORRHAGE ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OTORRHOEA ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PAROTITIS ( 1 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 1 FDA reports)
PERICARDIAL HAEMORRHAGE ( 1 FDA reports)
PERIPHERAL OCCLUSIVE DISEASE ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PHARYNGOTONSILLITIS ( 1 FDA reports)
PHLEBITIS ( 1 FDA reports)
PNEUMOCOCCAL INFECTION ( 1 FDA reports)
PNEUMONIA CRYPTOCOCCAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROCEDURAL SITE REACTION ( 1 FDA reports)
PRODUCT LABEL ISSUE ( 1 FDA reports)
PROLONGED LABOUR ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RADIATION PNEUMONITIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL ABSCESS ( 1 FDA reports)
RENAL ARTERY THROMBOSIS ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL INFARCT ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY RATE DECREASED ( 1 FDA reports)
RETAINED PLACENTA OR MEMBRANES ( 1 FDA reports)
RETINAL HAEMORRHAGE ( 1 FDA reports)
RIGHT ATRIAL DILATATION ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTAVIRUS INFECTION ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SEPSIS NEONATAL ( 1 FDA reports)
SHONE COMPLEX ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN HAEMORRHAGE ( 1 FDA reports)
SMALL FOR DATES BABY ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SYSTEMIC CANDIDA ( 1 FDA reports)
TEETHING ( 1 FDA reports)
TORSADE DE POINTES ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URETERIC OBSTRUCTION ( 1 FDA reports)
UTERINE INVERSION ( 1 FDA reports)
UTERINE OPERATION ( 1 FDA reports)
VANISHING BILE DUCT SYNDROME ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 1 FDA reports)
WOUND EVISCERATION ( 1 FDA reports)
X-RAY ABNORMAL ( 1 FDA reports)

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