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

INTERSTITIAL LUNG DISEASE ( 72 FDA reports)
PLATELET COUNT DECREASED ( 69 FDA reports)
ANAEMIA ( 52 FDA reports)
HAEMOGLOBIN DECREASED ( 47 FDA reports)
PYREXIA ( 47 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 43 FDA reports)
MALAISE ( 41 FDA reports)
STOMATITIS ( 41 FDA reports)
FEBRILE NEUTROPENIA ( 40 FDA reports)
PNEUMONIA ( 38 FDA reports)
NAUSEA ( 35 FDA reports)
NEUTROPHIL COUNT DECREASED ( 35 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 34 FDA reports)
NEOPLASM MALIGNANT ( 32 FDA reports)
NEUTROPENIA ( 29 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 29 FDA reports)
DECREASED APPETITE ( 28 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 27 FDA reports)
HERPES ZOSTER ( 26 FDA reports)
PLEURAL EFFUSION ( 26 FDA reports)
BLOOD CREATININE INCREASED ( 25 FDA reports)
VOMITING ( 25 FDA reports)
RASH ( 23 FDA reports)
FIBRIN D DIMER INCREASED ( 22 FDA reports)
FIBRIN DEGRADATION PRODUCTS INCREASED ( 22 FDA reports)
ILEUS ( 22 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 22 FDA reports)
SEPSIS ( 22 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 21 FDA reports)
NEOPLASM PROGRESSION ( 20 FDA reports)
BLOOD UREA INCREASED ( 19 FDA reports)
PAIN ( 19 FDA reports)
CONDITION AGGRAVATED ( 18 FDA reports)
DEEP VEIN THROMBOSIS ( 18 FDA reports)
DEHYDRATION ( 18 FDA reports)
DIARRHOEA ( 18 FDA reports)
LEUKOPENIA ( 18 FDA reports)
NASOPHARYNGITIS ( 18 FDA reports)
OVARIAN CANCER ( 18 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 18 FDA reports)
SHOCK ( 18 FDA reports)
OVARIAN CANCER RECURRENT ( 17 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 16 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 15 FDA reports)
BONE MARROW FAILURE ( 15 FDA reports)
CARDIAC FAILURE ( 15 FDA reports)
COUGH ( 15 FDA reports)
BLOOD BILIRUBIN INCREASED ( 14 FDA reports)
HYPERGLYCAEMIA ( 14 FDA reports)
INFECTION ( 14 FDA reports)
MELAENA ( 14 FDA reports)
MYALGIA ( 14 FDA reports)
PNEUMONIA ASPIRATION ( 14 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 13 FDA reports)
INTESTINAL OBSTRUCTION ( 13 FDA reports)
NEUROSIS ( 13 FDA reports)
PULMONARY OEDEMA ( 13 FDA reports)
RENAL IMPAIRMENT ( 13 FDA reports)
SKIN ULCER ( 13 FDA reports)
STAPHYLOCOCCAL INFECTION ( 13 FDA reports)
BLISTER ( 12 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 12 FDA reports)
FIBRIN DECREASED ( 12 FDA reports)
GASTRIC HAEMORRHAGE ( 12 FDA reports)
GASTROENTERITIS ( 12 FDA reports)
HAEMATOCRIT DECREASED ( 12 FDA reports)
HAEMOLYTIC ANAEMIA ( 12 FDA reports)
RETICULOCYTE COUNT INCREASED ( 12 FDA reports)
RETINAL HAEMORRHAGE ( 12 FDA reports)
DRUG INEFFECTIVE ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
ERYTHEMA ( 11 FDA reports)
THROMBOCYTOPENIA ( 11 FDA reports)
ASCITES ( 10 FDA reports)
CEREBRAL INFARCTION ( 10 FDA reports)
DEATH ( 10 FDA reports)
DIABETES MELLITUS ( 10 FDA reports)
EMBOLISM VENOUS ( 10 FDA reports)
INFUSION RELATED REACTION ( 10 FDA reports)
PERTUSSIS ( 10 FDA reports)
PHARYNGITIS ( 10 FDA reports)
VISUAL FIELD DEFECT ( 10 FDA reports)
ABNORMAL BEHAVIOUR ( 9 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 9 FDA reports)
BLOOD PRESSURE DECREASED ( 9 FDA reports)
CATARACT ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
DISEASE PROGRESSION ( 9 FDA reports)
DRY SKIN ( 9 FDA reports)
ENTEROCOLITIS ( 9 FDA reports)
ENTEROCOLITIS INFECTIOUS ( 9 FDA reports)
FALL ( 9 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 9 FDA reports)
GRAFT VERSUS HOST DISEASE ( 9 FDA reports)
HYPONATRAEMIA ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
ARRHYTHMIA ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
BLOOD MAGNESIUM DECREASED ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 8 FDA reports)
CELLULITIS ( 8 FDA reports)
EOSINOPHIL COUNT INCREASED ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
HYPOALBUMINAEMIA ( 8 FDA reports)
LIVER DISORDER ( 8 FDA reports)
LOSS OF CONSCIOUSNESS ( 8 FDA reports)
LYMPHOPENIA ( 8 FDA reports)
OEDEMA ( 8 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 8 FDA reports)
RESPIRATORY DISORDER ( 8 FDA reports)
VITRECTOMY ( 8 FDA reports)
ACNE ( 7 FDA reports)
ANGINA PECTORIS ( 7 FDA reports)
ARTERIOSPASM CORONARY ( 7 FDA reports)
ASTHENIA ( 7 FDA reports)
CANCER PAIN ( 7 FDA reports)
CARDIOVASCULAR DISORDER ( 7 FDA reports)
CATHETERISATION CARDIAC ( 7 FDA reports)
CONTUSION ( 7 FDA reports)
CORONARY ANGIOPLASTY ( 7 FDA reports)
CORONARY ARTERIAL STENT INSERTION ( 7 FDA reports)
CORONARY ARTERY STENOSIS ( 7 FDA reports)
DRUG ERUPTION ( 7 FDA reports)
DYSGEUSIA ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT DEPRESSION ( 7 FDA reports)
ELECTROCARDIOGRAM ST SEGMENT ELEVATION ( 7 FDA reports)
EXERCISE ELECTROCARDIOGRAM ABNORMAL ( 7 FDA reports)
EXERCISE TEST ABNORMAL ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
GASTROINTESTINAL PERFORATION ( 7 FDA reports)
GENERALISED OEDEMA ( 7 FDA reports)
GINGIVAL SWELLING ( 7 FDA reports)
LARYNGEAL OEDEMA ( 7 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 7 FDA reports)
MOUTH ULCERATION ( 7 FDA reports)
MYOCARDIAL ISCHAEMIA ( 7 FDA reports)
OTITIS MEDIA ( 7 FDA reports)
PAIN IN EXTREMITY ( 7 FDA reports)
RESPIRATORY FAILURE ( 7 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 7 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 7 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 7 FDA reports)
ABSCESS NECK ( 6 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 6 FDA reports)
ANGIOPATHY ( 6 FDA reports)
APPENDICITIS ( 6 FDA reports)
ARTERIOVENOUS FISTULA ( 6 FDA reports)
BLOOD BETA-D-GLUCAN INCREASED ( 6 FDA reports)
CHEST DISCOMFORT ( 6 FDA reports)
CONVULSION ( 6 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 6 FDA reports)
HAEMATURIA ( 6 FDA reports)
HEPATITIS B ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 6 FDA reports)
LYMPHADENITIS ( 6 FDA reports)
NEUROPATHY PERIPHERAL ( 6 FDA reports)
OFF LABEL USE ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
PNEUMONIA BACTERIAL ( 6 FDA reports)
PULMONARY HAEMORRHAGE ( 6 FDA reports)
RENAL FAILURE ( 6 FDA reports)
SKIN EROSION ( 6 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 6 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 5 FDA reports)
ALLERGIC TRANSFUSION REACTION ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
BACK PAIN ( 5 FDA reports)
BLOOD POTASSIUM DECREASED ( 5 FDA reports)
BRADYCARDIA ( 5 FDA reports)
BRONCHITIS ( 5 FDA reports)
CARDIOMEGALY ( 5 FDA reports)
CEREBRAL ISCHAEMIA ( 5 FDA reports)
CHILLS ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
EPIDERMOLYSIS BULLOSA ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 5 FDA reports)
HAEMATOCHEZIA ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPERSENSITIVITY ( 5 FDA reports)
HYPOGLYCAEMIA ( 5 FDA reports)
INTERVERTEBRAL DISCITIS ( 5 FDA reports)
MYOGLOBINURIA ( 5 FDA reports)
MYRINGITIS ( 5 FDA reports)
PANCREATITIS ACUTE ( 5 FDA reports)
PHOTOSENSITIVITY REACTION ( 5 FDA reports)
PROCTALGIA ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
TENDERNESS ( 5 FDA reports)
THERMAL BURN ( 5 FDA reports)
VASCULITIS ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
ACUTE GRAFT VERSUS HOST DISEASE IN LIVER ( 4 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 4 FDA reports)
ANAPHYLACTIC REACTION ( 4 FDA reports)
ANOREXIA ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
APATHY ( 4 FDA reports)
APTYALISM ( 4 FDA reports)
ASTHMA ( 4 FDA reports)
BACTERIAL INFECTION ( 4 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 4 FDA reports)
BUCCAL MUCOSAL ROUGHENING ( 4 FDA reports)
CATHETER SITE INFECTION ( 4 FDA reports)
CEREBRAL ATROPHY ( 4 FDA reports)
CHRONIC GRAFT VERSUS HOST DISEASE ( 4 FDA reports)
CORONARY ARTERY RESTENOSIS ( 4 FDA reports)
DIARRHOEA INFECTIOUS ( 4 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSPEPSIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
EATING DISORDER ( 4 FDA reports)
ENTEROCOLITIS VIRAL ( 4 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 4 FDA reports)
FOOD POISONING ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
GASTROINTESTINAL DISORDER ( 4 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 4 FDA reports)
GINGIVAL ERYTHEMA ( 4 FDA reports)
HAEMORRHAGE INTRACRANIAL ( 4 FDA reports)
HYPERKALAEMIA ( 4 FDA reports)
HYPOPHAGIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
IMPETIGO ( 4 FDA reports)
LACUNAR INFARCTION ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
LYMPH NODE ABSCESS ( 4 FDA reports)
LYMPH NODE PAIN ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
ORAL INFECTION ( 4 FDA reports)
PARONYCHIA ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PROTHROMBIN TIME PROLONGED ( 4 FDA reports)
PULMONARY EMBOLISM ( 4 FDA reports)
PYELONEPHRITIS ( 4 FDA reports)
PYODERMA GANGRENOSUM ( 4 FDA reports)
RESPIRATORY ARREST ( 4 FDA reports)
RESTLESSNESS ( 4 FDA reports)
TOXIC SKIN ERUPTION ( 4 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 4 FDA reports)
TUBERCULOSIS ( 4 FDA reports)
ULCER ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VENOOCCLUSIVE DISEASE ( 4 FDA reports)
ABDOMINAL MASS ( 3 FDA reports)
AORTIC DISSECTION ( 3 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 3 FDA reports)
BACTERAEMIA ( 3 FDA reports)
BLEPHARITIS ( 3 FDA reports)
BLOOD AMYLASE INCREASED ( 3 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
CENTRAL OBESITY ( 3 FDA reports)
CEREBRAL HAEMORRHAGE ( 3 FDA reports)
CHEST X-RAY ABNORMAL ( 3 FDA reports)
CUSHINGOID ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIABETIC KETOACIDOSIS ( 3 FDA reports)
EOSINOPHIL COUNT DECREASED ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYELID FUNCTION DISORDER ( 3 FDA reports)
EYELID OEDEMA ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
GASTRIC ULCER ( 3 FDA reports)
GINGIVITIS ( 3 FDA reports)
GLOSSITIS ( 3 FDA reports)
GRANULOCYTOPENIA ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEPATIC VEIN OCCLUSION ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 3 FDA reports)
INCISIONAL HERNIA ( 3 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 3 FDA reports)
METASTASES TO LIVER ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
MYCOPLASMA SEROLOGY POSITIVE ( 3 FDA reports)
MYOCARDIAL INFARCTION ( 3 FDA reports)
OESOPHAGEAL FISTULA ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
ONYCHOLYSIS ( 3 FDA reports)
ORAL INTAKE REDUCED ( 3 FDA reports)
OVERDOSE ( 3 FDA reports)
PARENTERAL NUTRITION ( 3 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 3 FDA reports)
PNEUMONITIS ( 3 FDA reports)
POLYARTERITIS NODOSA ( 3 FDA reports)
PROTEIN URINE PRESENT ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PYOMETRA ( 3 FDA reports)
RENAL CELL CARCINOMA ( 3 FDA reports)
RENAL INFARCT ( 3 FDA reports)
RENAL TUBULAR NECROSIS ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
SKIN DISORDER ( 3 FDA reports)
SOFT TISSUE NECROSIS ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
STENT PLACEMENT ( 3 FDA reports)
STRIDOR ( 3 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 3 FDA reports)
SWELLING FACE ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TENDON INJURY ( 3 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TUMOUR HAEMORRHAGE ( 3 FDA reports)
URTICARIA ( 3 FDA reports)
VALVULOPLASTY CARDIAC ( 3 FDA reports)
VIRAL INFECTION ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACUTE MYELOID LEUKAEMIA ( 2 FDA reports)
ANKLE FRACTURE ( 2 FDA reports)
ARTHRITIS REACTIVE ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
BRONCHOPULMONARY ASPERGILLOSIS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHOKING ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CYTOMEGALOVIRUS VIRAEMIA ( 2 FDA reports)
DEVICE RELATED INFECTION ( 2 FDA reports)
DIPLEGIA ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
ENCEPHALITIS FUNGAL ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
FACE OEDEMA ( 2 FDA reports)
FACIAL SPASM ( 2 FDA reports)
GASTROINTESTINAL OBSTRUCTION ( 2 FDA reports)
GASTROINTESTINAL STROMAL TUMOUR ( 2 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 2 FDA reports)
HEAD TITUBATION ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HERNIA REPAIR ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTENSION ( 2 FDA reports)
ILLUSION ( 2 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
JOINT DISLOCATION ( 2 FDA reports)
LICHEN PLANUS ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MALIGNANT ASCITES ( 2 FDA reports)
METASTASES TO BONE ( 2 FDA reports)
MOOD ALTERED ( 2 FDA reports)
MUCOSAL INFLAMMATION ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
NEPHROTIC SYNDROME ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORAL LICHEN PLANUS ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSMOTIC DEMYELINATION SYNDROME ( 2 FDA reports)
OTITIS EXTERNA ( 2 FDA reports)
PERFORMANCE STATUS DECREASED ( 2 FDA reports)
PERITONSILLAR ABSCESS ( 2 FDA reports)
PNEUMOCYSTIS TEST POSITIVE ( 2 FDA reports)
POST PROCEDURAL INFECTION ( 2 FDA reports)
PREGNANCY ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
RADIATION SKIN INJURY ( 2 FDA reports)
RECTAL STENOSIS ( 2 FDA reports)
RENAL ARTERY THROMBOSIS ( 2 FDA reports)
RESPIRATORY RATE INCREASED ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
SHOCK HAEMORRHAGIC ( 2 FDA reports)
SPUTUM RETENTION ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
THIRST ( 2 FDA reports)
TOOTH DISCOLOURATION ( 2 FDA reports)
TOOTH HYPOPLASIA ( 2 FDA reports)
TOOTH INJURY ( 2 FDA reports)
UNEVALUABLE EVENT ( 2 FDA reports)
WOUND DEHISCENCE ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABORTION ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACUTE CORONARY SYNDROME ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANAPHYLACTOID SHOCK ( 1 FDA reports)
ANXIETY DISORDER ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ASTERIXIS ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BIOPSY SKIN ABNORMAL ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRAIN STEM INFARCTION ( 1 FDA reports)
CARDIAC HYPERTROPHY ( 1 FDA reports)
CELL MARKER INCREASED ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHLAMYDIAL INFECTION ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLORECTAL CANCER ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY THROMBOSIS ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DUODENAL ULCER HAEMORRHAGE ( 1 FDA reports)
DUODENAL ULCER PERFORATION ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSLALIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE AMPLITUDE INCREASED ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
FALLOPIAN TUBE CANCER ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HYPERAMYLASAEMIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILIAC ARTERY OCCLUSION ( 1 FDA reports)
INJURY ( 1 FDA reports)
INTESTINAL FISTULA ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
LEUKOENCEPHALOPATHY ( 1 FDA reports)
LIPASE INCREASED ( 1 FDA reports)
LOWER LIMB FRACTURE ( 1 FDA reports)
LUNG CONSOLIDATION ( 1 FDA reports)
LUNG INFECTION PSEUDOMONAL ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOCYTE COUNT ( 1 FDA reports)
MALIGNANT PERITONEAL NEOPLASM ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYCOPLASMA INFECTION ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NORMAL NEWBORN ( 1 FDA reports)
ODYNOPHAGIA ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PANCREATIC NEUROENDOCRINE TUMOUR ( 1 FDA reports)
PERIPHERAL CIRCULATORY FAILURE ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERNICIOUS ANAEMIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHARYNGEAL DISORDER ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGEAL ULCERATION ( 1 FDA reports)
PNEUMONIA STAPHYLOCOCCAL ( 1 FDA reports)
PSEUDOMONAS TEST POSITIVE ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PUPILLARY REFLEX IMPAIRED ( 1 FDA reports)
RADIATION OESOPHAGITIS ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RENAL VASCULITIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SEBORRHOEIC DERMATITIS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TOXIC ENCEPHALOPATHY ( 1 FDA reports)
TREMOR ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VASCULAR PSEUDOANEURYSM ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)

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