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

PYREXIA ( 34 FDA reports)
NAUSEA ( 31 FDA reports)
MALAISE ( 29 FDA reports)
HYPOGLYCAEMIA ( 28 FDA reports)
BLOOD CREATININE INCREASED ( 27 FDA reports)
RHABDOMYOLYSIS ( 25 FDA reports)
BLOOD UREA INCREASED ( 23 FDA reports)
CARDIAC FAILURE ( 23 FDA reports)
ANAEMIA ( 21 FDA reports)
DECREASED APPETITE ( 20 FDA reports)
CEREBRAL INFARCTION ( 19 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 19 FDA reports)
PNEUMONIA ( 19 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 18 FDA reports)
DEHYDRATION ( 18 FDA reports)
PLATELET COUNT DECREASED ( 18 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 18 FDA reports)
HAEMODIALYSIS ( 17 FDA reports)
RENAL IMPAIRMENT ( 17 FDA reports)
CONDITION AGGRAVATED ( 16 FDA reports)
RASH ( 16 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 15 FDA reports)
HYPOAESTHESIA ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
VITREOUS HAEMORRHAGE ( 15 FDA reports)
VOMITING ( 15 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 14 FDA reports)
ATRIOVENTRICULAR BLOCK SECOND DEGREE ( 14 FDA reports)
NEPHROTIC SYNDROME ( 14 FDA reports)
RENAL FAILURE ACUTE ( 14 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 13 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 13 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 13 FDA reports)
DRUG INEFFECTIVE ( 13 FDA reports)
HYPERKALAEMIA ( 13 FDA reports)
ILEUS ( 13 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 12 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 12 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 12 FDA reports)
DRUG INTERACTION ( 12 FDA reports)
HYPERTENSION ( 12 FDA reports)
ANOREXIA ( 11 FDA reports)
DIARRHOEA ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
FEELING COLD ( 11 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 11 FDA reports)
INFECTION ( 11 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE III ( 11 FDA reports)
OVERDOSE ( 11 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 11 FDA reports)
URINARY TRACT INFECTION ( 11 FDA reports)
HEPATIC FAILURE ( 10 FDA reports)
PROTEIN URINE PRESENT ( 10 FDA reports)
RENAL FAILURE ( 10 FDA reports)
RESTLESSNESS ( 10 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
ANGINA PECTORIS ( 9 FDA reports)
ASTHENIA ( 9 FDA reports)
BLOOD SODIUM DECREASED ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
DYSPNOEA ( 9 FDA reports)
FALL ( 9 FDA reports)
INTERSTITIAL LUNG DISEASE ( 9 FDA reports)
PLEURAL EFFUSION ( 9 FDA reports)
RENAL FAILURE CHRONIC ( 9 FDA reports)
URINARY RETENTION ( 9 FDA reports)
ANAPHYLACTIC SHOCK ( 8 FDA reports)
ATRIAL FIBRILLATION ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 8 FDA reports)
CARDIO-RESPIRATORY ARREST ( 8 FDA reports)
CEREBELLAR HAEMORRHAGE ( 8 FDA reports)
CONSTIPATION ( 8 FDA reports)
DEATH ( 8 FDA reports)
DIABETIC NEPHROPATHY ( 8 FDA reports)
DIZZINESS ( 8 FDA reports)
GAIT DISTURBANCE ( 8 FDA reports)
HAEMOGLOBIN DECREASED ( 8 FDA reports)
HEADACHE ( 8 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 8 FDA reports)
LUNG DISORDER ( 8 FDA reports)
PANCREATITIS ACUTE ( 8 FDA reports)
RENAL DISORDER ( 8 FDA reports)
SEPSIS ( 8 FDA reports)
STAPHYLOCOCCAL INFECTION ( 8 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 8 FDA reports)
URINE OUTPUT DECREASED ( 8 FDA reports)
WEIGHT INCREASED ( 8 FDA reports)
BILE DUCT CANCER ( 7 FDA reports)
CARDIAC ARREST ( 7 FDA reports)
CEREBRAL HAEMORRHAGE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
HERPES ZOSTER ( 7 FDA reports)
PANCYTOPENIA ( 7 FDA reports)
RETINAL HAEMORRHAGE ( 7 FDA reports)
SOMNOLENCE ( 7 FDA reports)
SYNCOPE ( 7 FDA reports)
ACUTE HEPATIC FAILURE ( 6 FDA reports)
COLON ADENOMA ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
GLUCOSE URINE PRESENT ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
HYPONATRAEMIA ( 6 FDA reports)
LEUKOPENIA ( 6 FDA reports)
LIVER DISORDER ( 6 FDA reports)
OEDEMA ( 6 FDA reports)
PARALYSIS ( 6 FDA reports)
POLLAKIURIA ( 6 FDA reports)
SPEECH DISORDER ( 6 FDA reports)
URTICARIA ( 6 FDA reports)
ANHIDROSIS ( 5 FDA reports)
APHASIA ( 5 FDA reports)
BLOOD POTASSIUM INCREASED ( 5 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 5 FDA reports)
BODY TEMPERATURE INCREASED ( 5 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 5 FDA reports)
CARDIOVASCULAR DISORDER ( 5 FDA reports)
DYSSTASIA ( 5 FDA reports)
ENCEPHALOPATHY ( 5 FDA reports)
EPISTAXIS ( 5 FDA reports)
ERYTHEMA ( 5 FDA reports)
ERYTHEMA MULTIFORME ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HALLUCINATION ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPERTRIGLYCERIDAEMIA ( 5 FDA reports)
INTERVERTEBRAL DISCITIS ( 5 FDA reports)
KAPOSI'S SARCOMA ( 5 FDA reports)
LARGE INTESTINE CARCINOMA ( 5 FDA reports)
LOSS OF CONSCIOUSNESS ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 5 FDA reports)
OLIGURIA ( 5 FDA reports)
POST PROCEDURAL COMPLICATION ( 5 FDA reports)
PROTEINURIA ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
RASH GENERALISED ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 5 FDA reports)
SPONDYLITIS ( 5 FDA reports)
STOMATITIS ( 5 FDA reports)
ACUTE LEUKAEMIA ( 4 FDA reports)
ANURIA ( 4 FDA reports)
APLASTIC ANAEMIA ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 4 FDA reports)
DISEASE PROGRESSION ( 4 FDA reports)
DISORIENTATION ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
DYSLALIA ( 4 FDA reports)
DYSURIA ( 4 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX PROLONGED ( 4 FDA reports)
ENTEROCOLITIS ( 4 FDA reports)
FACE OEDEMA ( 4 FDA reports)
FEELING ABNORMAL ( 4 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 4 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 4 FDA reports)
HAEMATEMESIS ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HEMIPLEGIA ( 4 FDA reports)
HISTIOCYTOSIS HAEMATOPHAGIC ( 4 FDA reports)
HYPERGLYCAEMIA ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
HYPOXIA ( 4 FDA reports)
LIPOMA ( 4 FDA reports)
LOGORRHOEA ( 4 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 4 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 4 FDA reports)
MULTI-ORGAN FAILURE ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
MYOCLONUS ( 4 FDA reports)
NASOPHARYNGITIS ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PARALYSIS FLACCID ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PROSTATE CANCER ( 4 FDA reports)
PSYCHIATRIC SYMPTOM ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
TACHYCARDIA ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABDOMINAL PAIN UPPER ( 3 FDA reports)
ACUTE CORONARY SYNDROME ( 3 FDA reports)
ACUTE PRERENAL FAILURE ( 3 FDA reports)
ALCOHOL USE ( 3 FDA reports)
APNOEIC ATTACK ( 3 FDA reports)
ARTHRALGIA ( 3 FDA reports)
ASCITES ( 3 FDA reports)
AZOTAEMIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BLADDER DISORDER ( 3 FDA reports)
BLOOD ALBUMIN DECREASED ( 3 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 3 FDA reports)
CANDIDIASIS ( 3 FDA reports)
CHOLECYSTITIS ACUTE ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
COLITIS ( 3 FDA reports)
DRUG ERUPTION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
ECZEMA ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
FAECES DISCOLOURED ( 3 FDA reports)
GASTRITIS ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GLUCOSE URINE ( 3 FDA reports)
HEMIPARESIS ( 3 FDA reports)
HYPOCALCAEMIA ( 3 FDA reports)
HYPOGLYCAEMIC COMA ( 3 FDA reports)
ILEUS PARALYTIC ( 3 FDA reports)
INFLUENZA ( 3 FDA reports)
INJURY ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LYMPHANGIOSIS CARCINOMATOSA ( 3 FDA reports)
MALABSORPTION ( 3 FDA reports)
METASTASES TO LUNG ( 3 FDA reports)
MOTOR DYSFUNCTION ( 3 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 3 FDA reports)
MYOCARDIAL ISCHAEMIA ( 3 FDA reports)
NEUROSIS ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
OROPHARYNGITIS FUNGAL ( 3 FDA reports)
OSTEOMYELITIS ( 3 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 3 FDA reports)
PARESIS ( 3 FDA reports)
PHOTOSENSITIVITY REACTION ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
PULMONARY CONGESTION ( 3 FDA reports)
PULMONARY OEDEMA ( 3 FDA reports)
PURPURA ( 3 FDA reports)
PYELONEPHRITIS ( 3 FDA reports)
STILL'S DISEASE ADULT ONSET ( 3 FDA reports)
SUICIDE ATTEMPT ( 3 FDA reports)
SUPERIOR SAGITTAL SINUS THROMBOSIS ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
THROMBOCYTOPENIA ( 3 FDA reports)
THROMBOTIC STROKE ( 3 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 3 FDA reports)
ABDOMINAL PAIN LOWER ( 2 FDA reports)
ACIDOSIS ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANAEMIA OF CHRONIC DISEASE ( 2 FDA reports)
ANORECTAL DISORDER ( 2 FDA reports)
ANTI-INSULIN ANTIBODY ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL HAEMORRHAGE ( 2 FDA reports)
ASPIRATION ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK ( 2 FDA reports)
ATRIOVENTRICULAR BLOCK FIRST DEGREE ( 2 FDA reports)
BILE DUCT STONE ( 2 FDA reports)
BLADDER DYSFUNCTION ( 2 FDA reports)
BLISTER ( 2 FDA reports)
BLOOD CHOLESTEROL DECREASED ( 2 FDA reports)
BLOOD CREATININE ( 2 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 2 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES DECREASED ( 2 FDA reports)
BLOOD URINE ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BONE MARROW FAILURE ( 2 FDA reports)
CAROTID ARTERY STENOSIS ( 2 FDA reports)
CEREBROVASCULAR DISORDER ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COLITIS ULCERATIVE ( 2 FDA reports)
COLORECTAL CANCER ( 2 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 2 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 2 FDA reports)
CONVERSION DISORDER ( 2 FDA reports)
COUGH ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DECUBITUS ULCER ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ACNEIFORM ( 2 FDA reports)
DERMATITIS BULLOUS ( 2 FDA reports)
DERMATITIS EXFOLIATIVE ( 2 FDA reports)
DIABETIC GANGRENE ( 2 FDA reports)
DIABETIC RETINOPATHY ( 2 FDA reports)
DRUG ADMINISTRATION ERROR ( 2 FDA reports)
DRUG TOXICITY ( 2 FDA reports)
DYSCHEZIA ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
EAR PAIN ( 2 FDA reports)
EATING DISORDER ( 2 FDA reports)
ELECTROCARDIOGRAM PQ INTERVAL PROLONGED ( 2 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 2 FDA reports)
ENDOCARDITIS ( 2 FDA reports)
EOSINOPHIL COUNT DECREASED ( 2 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROINTESTINAL OEDEMA ( 2 FDA reports)
GINGIVAL HYPERTROPHY ( 2 FDA reports)
GINGIVECTOMY ( 2 FDA reports)
HAEMATOMA ( 2 FDA reports)
HALLUCINATIONS, MIXED ( 2 FDA reports)
HEAD INJURY ( 2 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERPARATHYROIDISM SECONDARY ( 2 FDA reports)
HYPERTHERMIA MALIGNANT ( 2 FDA reports)
HYPERURICAEMIA ( 2 FDA reports)
HYPOCHLORAEMIA ( 2 FDA reports)
HYPOCHROMIC ANAEMIA ( 2 FDA reports)
HYPOMAGNESAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
IMMUNE SYSTEM DISORDER ( 2 FDA reports)
INCOHERENT ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LABORATORY TEST ABNORMAL ( 2 FDA reports)
LIP HAEMORRHAGE ( 2 FDA reports)
LYMPHOMA ( 2 FDA reports)
MUCOUS STOOLS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NECROSIS ( 2 FDA reports)
NEPHROGENIC DIABETES INSIPIDUS ( 2 FDA reports)
NEPHROPATHY ( 2 FDA reports)
NEURODEGENERATIVE DISORDER ( 2 FDA reports)
NEUTROPHIL COUNT DECREASED ( 2 FDA reports)
OEDEMA MUCOSAL ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PAROSMIA ( 2 FDA reports)
PELVIC FLUID COLLECTION ( 2 FDA reports)
PERICORONITIS ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PIGMENTATION DISORDER ( 2 FDA reports)
POLYURIA ( 2 FDA reports)
PORPHYRIA ACUTE ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PULSE ABSENT ( 2 FDA reports)
RENAL CELL CARCINOMA ( 2 FDA reports)
RENAL TUBULAR ACIDOSIS ( 2 FDA reports)
RESPIRATORY RATE DECREASED ( 2 FDA reports)
RETINAL VEIN OCCLUSION ( 2 FDA reports)
RETROPERITONEAL ABSCESS ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SEPTIC SHOCK ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SIGMOIDECTOMY ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SKIN EXFOLIATION ( 2 FDA reports)
SKIN OEDEMA ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STREPTOCOCCAL INFECTION ( 2 FDA reports)
TACHYCARDIA PAROXYSMAL ( 2 FDA reports)
TOOTH EXTRACTION ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
UNRESPONSIVE TO VERBAL STIMULI ( 2 FDA reports)
URINARY CASTS ( 2 FDA reports)
URINARY INCONTINENCE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
VOLVULUS ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANAPHYLACTOID REACTION ( 1 FDA reports)
ANTI-INSULIN ANTIBODY POSITIVE ( 1 FDA reports)
ANTIBIOTIC RESISTANT STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
AORTIC DISSECTION RUPTURE ( 1 FDA reports)
APATHY ( 1 FDA reports)
APLASIA PURE RED CELL ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATYPICAL MYCOBACTERIAL INFECTION ( 1 FDA reports)
AUTONOMIC NERVOUS SYSTEM IMBALANCE ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT CANCER STAGE III ( 1 FDA reports)
BILIRUBINURIA ( 1 FDA reports)
BK VIRUS INFECTION ( 1 FDA reports)
BLOOD CALCIUM ABNORMAL ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC ABNORMAL ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
CANCER PAIN ( 1 FDA reports)
CARDIAC DEATH ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL VENOUS PRESSURE INCREASED ( 1 FDA reports)
CEREBRAL DISORDER ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CRUSH INJURY ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DUODENAL ULCER ( 1 FDA reports)
ENTERITIS INFECTIOUS ( 1 FDA reports)
EOSINOPHIL COUNT INCREASED ( 1 FDA reports)
EOSINOPHIL PERCENTAGE INCREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EVAN'S SYNDROME ( 1 FDA reports)
EWING'S SARCOMA ( 1 FDA reports)
EXANTHEM ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FIBRIN D DIMER DECREASED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOCAL GLOMERULOSCLEROSIS ( 1 FDA reports)
FOOD CRAVING ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC PERFORATION ( 1 FDA reports)
GASTROINTESTINAL EROSION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 1 FDA reports)
GLOMERULONEPHRITIS CHRONIC ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HUMERUS FRACTURE ( 1 FDA reports)
HYPERBILIRUBINAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOMETABOLISM ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOPHOSPHATAEMIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFECTED EPIDERMAL CYST ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE RASH ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
INTESTINAL CYST ( 1 FDA reports)
INTESTINAL MUCOSAL ATROPHY ( 1 FDA reports)
INTESTINAL PERFORATION ( 1 FDA reports)
INTESTINAL STENOSIS ( 1 FDA reports)
INTESTINAL VILLI ATROPHY ( 1 FDA reports)
INTRACARDIAC THROMBUS ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LARYNGEAL OEDEMA ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIMB SALVAGE THERAPY ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MACULAR OEDEMA ( 1 FDA reports)
MENTAL STATUS CHANGES ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTATIC CARCINOMA OF THE BLADDER ( 1 FDA reports)
MICROCYTIC ANAEMIA ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NEOPLASM GROWTH ACCELERATED ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEPHRITIS ( 1 FDA reports)
NEPHRITIS INTERSTITIAL ( 1 FDA reports)
NEPHROGENIC ANAEMIA ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPENIC COLITIS ( 1 FDA reports)
NEUTROPHIL COUNT ABNORMAL ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OPHTHALMOPLEGIA ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANIC DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMATOSIS CYSTOIDES INTESTINALIS ( 1 FDA reports)
PNEUMOCOCCAL SEPSIS ( 1 FDA reports)
PNEUMOCYSTIS JIROVECI PNEUMONIA ( 1 FDA reports)
PNEUMONIA KLEBSIELLA ( 1 FDA reports)
PROCALCITONIN INCREASED ( 1 FDA reports)
PROTHROMBIN TIME SHORTENED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 1 FDA reports)
PULMONARY ARTERIAL WEDGE PRESSURE INCREASED ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RETINAL ANEURYSM ( 1 FDA reports)
RETINAL EXUDATES ( 1 FDA reports)
RETINOPATHY PROLIFERATIVE ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPINAL COMPRESSION FRACTURE ( 1 FDA reports)
STAPHYLOCOCCUS TEST POSITIVE ( 1 FDA reports)
STRESS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
THROMBOTIC THROMBOCYTOPENIC PURPURA ( 1 FDA reports)
TRANSPLANT REJECTION ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
TUMOUR ASSOCIATED FEVER ( 1 FDA reports)
TUMOUR EXCISION ( 1 FDA reports)
URETERAL CATHETERISATION ( 1 FDA reports)
VARICES OESOPHAGEAL ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VITAMIN K DEFICIENCY ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)
XANTHOPSIA ( 1 FDA reports)

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