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

PYREXIA ( 25 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
RENAL FAILURE ( 15 FDA reports)
DIARRHOEA ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
DYSPNOEA ( 14 FDA reports)
MALAISE ( 14 FDA reports)
RASH ( 14 FDA reports)
AGRANULOCYTOSIS ( 12 FDA reports)
ANAEMIA ( 12 FDA reports)
INFECTION ( 12 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 10 FDA reports)
HAEMOGLOBIN DECREASED ( 10 FDA reports)
PLATELET COUNT DECREASED ( 10 FDA reports)
STOMATITIS ( 10 FDA reports)
DIZZINESS ( 9 FDA reports)
HAEMODIALYSIS ( 9 FDA reports)
HYPOGAMMAGLOBULINAEMIA ( 9 FDA reports)
LOSS OF CONSCIOUSNESS ( 9 FDA reports)
PRURITUS ( 9 FDA reports)
RENAL IMPAIRMENT ( 9 FDA reports)
STEVENS-JOHNSON SYNDROME ( 9 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 9 FDA reports)
BLOOD CREATININE INCREASED ( 8 FDA reports)
BLOOD URIC ACID INCREASED ( 8 FDA reports)
CEREBRAL INFARCTION ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DEHYDRATION ( 8 FDA reports)
MULTI-ORGAN FAILURE ( 8 FDA reports)
NAUSEA ( 8 FDA reports)
PANCYTOPENIA ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
VOMITING ( 8 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 8 FDA reports)
ALOPECIA ( 7 FDA reports)
BRADYCARDIA ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
HYPOAESTHESIA ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
OVERDOSE ( 7 FDA reports)
RHABDOMYOLYSIS ( 7 FDA reports)
SHOCK ( 7 FDA reports)
STAPHYLOCOCCAL INFECTION ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
ANOREXIA ( 6 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 6 FDA reports)
BLOOD PRESSURE DECREASED ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
COUGH ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DIALYSIS ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
HYPOGLYCAEMIA ( 6 FDA reports)
HYPOTENSION ( 6 FDA reports)
PLEURAL EFFUSION ( 6 FDA reports)
RESPIRATORY FAILURE ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
ALVEOLITIS ( 5 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 5 FDA reports)
BLOOD UREA INCREASED ( 5 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 5 FDA reports)
DISTURBANCE IN ATTENTION ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
INTERSTITIAL LUNG DISEASE ( 5 FDA reports)
JAUNDICE ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
BONE MARROW DEPRESSION ( 4 FDA reports)
BREAST CANCER ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CEREBRAL HAEMORRHAGE ( 4 FDA reports)
CHOLESTASIS ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
ECZEMA ( 4 FDA reports)
GAIT DISTURBANCE ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HAEMOPTYSIS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HEPATIC ENZYME INCREASED ( 4 FDA reports)
HEPATITIS FULMINANT ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOKALAEMIA ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
LEUKOPENIA ( 4 FDA reports)
MYOCARDIAL INFARCTION ( 4 FDA reports)
OSTEOPOROSIS ( 4 FDA reports)
PERIODONTITIS ( 4 FDA reports)
PLATELET COUNT INCREASED ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
POOR QUALITY SLEEP ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PROTHROMBIN TIME SHORTENED ( 4 FDA reports)
PSEUDOMONAS INFECTION ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RENAL DISORDER ( 4 FDA reports)
RENAL FAILURE CHRONIC ( 4 FDA reports)
SCAR ( 4 FDA reports)
SKIN REACTION ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
VASODILATATION ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
APHASIA ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ATRIAL FIBRILLATION ( 3 FDA reports)
ATRIOVENTRICULAR BLOCK ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BONE MARROW FAILURE ( 3 FDA reports)
CARDIOMYOPATHY ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DEEP VEIN THROMBOSIS ( 3 FDA reports)
DELIRIUM ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EMBOLISM ( 3 FDA reports)
ENTEROBACTER INFECTION ( 3 FDA reports)
FACE OEDEMA ( 3 FDA reports)
FALL ( 3 FDA reports)
FEELING ABNORMAL ( 3 FDA reports)
FUNGUS SEROLOGY TEST POSITIVE ( 3 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 3 FDA reports)
GRANULOMA ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMATOMA ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
HEPATIC FAILURE ( 3 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
INFARCTION ( 3 FDA reports)
LEUKOCYTOSIS ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
METABOLIC ALKALOSIS ( 3 FDA reports)
MUSCLE CRAMP ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NEPHRITIS INTERSTITIAL ( 3 FDA reports)
NEPHROPATHY TOXIC ( 3 FDA reports)
NERVOUS SYSTEM DISORDER ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PAIN ( 3 FDA reports)
PERIPHERAL ISCHAEMIA ( 3 FDA reports)
PERITONITIS ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PULMONARY TUBERCULOSIS ( 3 FDA reports)
PURPURA ( 3 FDA reports)
REFLUX OESOPHAGITIS ( 3 FDA reports)
SEPTIC SHOCK ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 3 FDA reports)
TROPONIN INCREASED ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ALPHA 1 GLOBULIN INCREASED ( 2 FDA reports)
ALPHA 2 GLOBULIN INCREASED ( 2 FDA reports)
ANAEMIA MACROCYTIC ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 2 FDA reports)
ANURIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BACTERIAL INFECTION ( 2 FDA reports)
BETA GLOBULIN ABNORMAL ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLADDER PAIN ( 2 FDA reports)
BLOOD ALBUMIN DECREASED ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD AMYLASE INCREASED ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CHOLINESTERASE DECREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRAIN SCAN ABNORMAL ( 2 FDA reports)
BRAIN STEM INFARCTION ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CARDIOVASCULAR DISORDER ( 2 FDA reports)
CIRCULATORY COLLAPSE ( 2 FDA reports)
CSF CELL COUNT INCREASED ( 2 FDA reports)
CSF PROTEIN INCREASED ( 2 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 2 FDA reports)
DIFFERENTIAL WHITE BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
DYSURIA ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
EOSINOPHILIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
EPSTEIN-BARR VIRUS INFECTION ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
FAECES HARD ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL PERFORATION ( 2 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 2 FDA reports)
GOUT ( 2 FDA reports)
HAEMATURIA ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATITIS ACUTE ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
HEPATOSPLENOMEGALY ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERPROLACTINAEMIA ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOALDOSTERONISM ( 2 FDA reports)
HYPOGLYCAEMIC COMA ( 2 FDA reports)
HYPOXIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
INFECTED SKIN ULCER ( 2 FDA reports)
INFECTION IN AN IMMUNOCOMPROMISED HOST ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO ABNORMAL ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LARGE INTESTINE PERFORATION ( 2 FDA reports)
LEUKOENCEPHALOPATHY ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
LUNG NEOPLASM ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEDICATION RESIDUE ( 2 FDA reports)
MENSTRUATION IRREGULAR ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MOUTH BREATHING ( 2 FDA reports)
MUSCLE HAEMORRHAGE ( 2 FDA reports)
MYOCARDIAL ISCHAEMIA ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 2 FDA reports)
OLIGURIA ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
OSTEOMYELITIS ( 2 FDA reports)
OXYGEN SATURATION DECREASED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PETECHIAE ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PITTING OEDEMA ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
POLYP ( 2 FDA reports)
PROTHROMBIN TIME ABNORMAL ( 2 FDA reports)
PSEUDO-BARTTER SYNDROME ( 2 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 2 FDA reports)
RED BLOOD CELL COUNT ABNORMAL ( 2 FDA reports)
RED BLOOD CELLS SEMEN POSITIVE ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL CYST ( 2 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHEUMATOID FACTOR POSITIVE ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SERUM FERRITIN INCREASED ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
STATUS ASTHMATICUS ( 2 FDA reports)
SUBCUTANEOUS ABSCESS ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VASCULAR PURPURA ( 2 FDA reports)
VASCULITIS ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACCESSORY SPLEEN ( 1 FDA reports)
ACQUIRED PYLORIC STENOSIS ( 1 FDA reports)
ACROCHORDON ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADENOCARCINOMA ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
ANAEMIA FOLATE DEFICIENCY ( 1 FDA reports)
ANAEMIA VITAMIN B12 DEFICIENCY ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC ATHEROSCLEROSIS ( 1 FDA reports)
AORTIC DILATATION ( 1 FDA reports)
AORTIC DISSECTION ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIOPATHIC DISEASE ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL TACHYCARDIA ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 1 FDA reports)
ATROPHY ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
AXILLARY PAIN ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BIOPSY LIVER ABNORMAL ( 1 FDA reports)
BLADDER DISTENSION ( 1 FDA reports)
BLOOD BLISTER ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN A INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN G INCREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN M INCREASED ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN OEDEMA ( 1 FDA reports)
BRONCHIAL INFECTION ( 1 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CALCULUS URETERIC ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARCINOID TUMOUR OF THE GASTROINTESTINAL TRACT ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC ASTHMA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIAC MURMUR ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOPULMONARY FAILURE ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CATHETER BACTERAEMIA ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CENTRAL LINE INFECTION ( 1 FDA reports)
CENTRAL VENOUS PRESSURE DECREASED ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHEMOTHERAPY ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLANGITIS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLEDOCHOLITHOTOMY ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CLEFT LIP AND PALATE ( 1 FDA reports)
COLECTOMY PARTIAL ( 1 FDA reports)
COLOBOMA ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COLON POLYPECTOMY ( 1 FDA reports)
COMA ( 1 FDA reports)
COMPLEMENT FACTOR DECREASED ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONCOMITANT DISEASE AGGRAVATED ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONGENITAL DIAPHRAGMATIC ANOMALY ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COOMBS POSITIVE HAEMOLYTIC ANAEMIA ( 1 FDA reports)
CRYING ( 1 FDA reports)
CRYOGLOBULINAEMIA ( 1 FDA reports)
CRYOGLOBULINS PRESENT ( 1 FDA reports)
CRYPTORCHISM ( 1 FDA reports)
CULTURE STOOL POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS ANTIGEN POSITIVE ( 1 FDA reports)
CYTOMEGALOVIRUS CHORIORETINITIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DENTAL TREATMENT ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMATITIS EXFOLIATIVE ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 1 FDA reports)
DIAPHRAGMATIC HERNIA ( 1 FDA reports)
DIFFUSE LARGE B-CELL LYMPHOMA ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISINHIBITION ( 1 FDA reports)
DISSEMINATED TUBERCULOSIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVERTICULUM INTESTINAL ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG INTOLERANCE ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DRUG RASH WITH EOSINOPHILIA AND SYSTEMIC SYMPTOMS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
ENDOMETRITIS ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
ENTEROCOCCAL BACTERAEMIA ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
ENTEROCOLITIS ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EPIDERMAL NECROSIS ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
ERYSIPELAS ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EXTERNAL AUDITORY CANAL ATRESIA ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
FAECAL VOLUME INCREASED ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FOETAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
FOLLICULITIS ( 1 FDA reports)
GASTRIC CANCER ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GENERALISED OEDEMA ( 1 FDA reports)
GENITAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOMERULONEPHRITIS ( 1 FDA reports)
GLOMERULONEPHRITIS MEMBRANOPROLIFERATIVE ( 1 FDA reports)
GLOMERULONEPHRITIS PROLIFERATIVE ( 1 FDA reports)
GLOSSOPTOSIS ( 1 FDA reports)
GRAFT VERSUS HOST DISEASE ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMORRHAGIC ASCITES ( 1 FDA reports)
HAEMORRHAGIC DISORDER ( 1 FDA reports)
HEAD DISCOMFORT ( 1 FDA reports)
HEART INJURY ( 1 FDA reports)
HELICOBACTER PYLORI IDENTIFICATION TEST POSITIVE ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC HAEMORRHAGE ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HIP ARTHROPLASTY ( 1 FDA reports)
HYDROCEPHALUS ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERGLOBULINAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERTELORISM OF ORBIT ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOCOAGULABLE STATE ( 1 FDA reports)
HYPOPROTHROMBINAEMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
ILEUS PARALYTIC ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
IMMUNODEFICIENCY ( 1 FDA reports)
IMPAIRED HEALING ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO FLUCTUATION ( 1 FDA reports)
INTERVERTEBRAL DISC CALCIFICATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTESTINAL HYPOMOTILITY ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
JAW OPERATION ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT SPRAIN ( 1 FDA reports)
KIDNEY ENLARGEMENT ( 1 FDA reports)
KLEBSIELLA INFECTION ( 1 FDA reports)
KNEE ARTHROPLASTY ( 1 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 1 FDA reports)
LARYNGEAL PAIN ( 1 FDA reports)
LAXATIVE ABUSE ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOCAL REACTION ( 1 FDA reports)
LOCALISED EXFOLIATION ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY MEDIASTINAL ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTE MORPHOLOGY ABNORMAL ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MALIGNANT ASCITES ( 1 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 1 FDA reports)
MEAN ARTERIAL PRESSURE DECREASED ( 1 FDA reports)
MEAN CELL VOLUME DECREASED ( 1 FDA reports)
MEAN PLATELET VOLUME DECREASED ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MELAENA ( 1 FDA reports)
MELANOSIS ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENISCUS LESION ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
METASTASES TO CENTRAL NERVOUS SYSTEM ( 1 FDA reports)
METASTASES TO MENINGES ( 1 FDA reports)
METASTASIS ( 1 FDA reports)
MICROPHTHALMOS ( 1 FDA reports)
MICROTIA ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCLE RUPTURE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOGLOBINURIA ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECROTISING FASCIITIS ( 1 FDA reports)
NEISSERIA INFECTION ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEUTROPENIC SEPSIS ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE DRUG EFFECT ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA DUE TO CARDIAC DISEASE ( 1 FDA reports)
OESOPHAGEAL CANDIDIASIS ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OPTIC ATROPHY ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL LICHEN PLANUS ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OSTEOMYELITIS CHRONIC ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVARIAN NEOPLASM ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC DISORDER ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANEOPLASTIC SYNDROME ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PERICARDITIS MALIGNANT ( 1 FDA reports)
PERITONEAL TUBERCULOSIS ( 1 FDA reports)
PHOSPHENES ( 1 FDA reports)
PHOTOSENSITIVITY REACTION ( 1 FDA reports)
PLEURAL DISORDER ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PNEUMOTHORAX ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYURIA ( 1 FDA reports)
POSITRON EMISSION TOMOGRAM ABNORMAL ( 1 FDA reports)
POST PROCEDURAL DIARRHOEA ( 1 FDA reports)
POSTRENAL FAILURE ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PROTEIN TOTAL INCREASED ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 1 FDA reports)
PSYCHOMOTOR RETARDATION ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL ATROPHY ( 1 FDA reports)
RENAL INJURY ( 1 FDA reports)
RENAL TUBULAR DISORDER ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RETICULOENDOTHELIAL SYSTEM STIMULATED ( 1 FDA reports)
RETROPERITONEAL ABSCESS ( 1 FDA reports)
RHEUMATOID LUNG ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SALPINGITIS TUBERCULOUS ( 1 FDA reports)
SCOTOMA ( 1 FDA reports)
SELF-MEDICATION ( 1 FDA reports)
SEQUESTRECTOMY ( 1 FDA reports)
SINGLE FUNCTIONAL KIDNEY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SOFT TISSUE INJURY ( 1 FDA reports)
SPINAL CORD DISORDER ( 1 FDA reports)
SPLENIC INFARCTION ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STAPHYLOCOCCAL BACTERAEMIA ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
SYSTOLIC HYPERTENSION ( 1 FDA reports)
T-CELL DEPLETION ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THIRST ( 1 FDA reports)
TONGUE PARALYSIS ( 1 FDA reports)
TONSILLITIS ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TROPONIN T INCREASED ( 1 FDA reports)
TUMOUR MARKER INCREASED ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 1 FDA reports)
URETHRITIS ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
UROBILIN URINE ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VITAMIN K INCREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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