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

DEPRESSED LEVEL OF CONSCIOUSNESS ( 26 FDA reports)
PYREXIA ( 25 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 22 FDA reports)
DIZZINESS ( 21 FDA reports)
MALAISE ( 20 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 19 FDA reports)
PNEUMONIA ( 18 FDA reports)
VOMITING ( 18 FDA reports)
CEREBRAL INFARCTION ( 17 FDA reports)
RENAL FAILURE ACUTE ( 17 FDA reports)
RENAL IMPAIRMENT ( 17 FDA reports)
BLOOD CREATININE INCREASED ( 16 FDA reports)
BLOOD UREA INCREASED ( 16 FDA reports)
FALL ( 16 FDA reports)
HAEMOGLOBIN DECREASED ( 16 FDA reports)
LOSS OF CONSCIOUSNESS ( 16 FDA reports)
PLATELET COUNT DECREASED ( 16 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 15 FDA reports)
ENCEPHALOPATHY ( 15 FDA reports)
HYPOGLYCAEMIA ( 15 FDA reports)
RENAL FAILURE ( 15 FDA reports)
RHABDOMYOLYSIS ( 15 FDA reports)
GASTRIC ULCER ( 13 FDA reports)
ANAEMIA ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
PAIN ( 12 FDA reports)
DEATH ( 11 FDA reports)
DYSARTHRIA ( 11 FDA reports)
DYSPNOEA ( 11 FDA reports)
INSOMNIA ( 11 FDA reports)
INTERSTITIAL LUNG DISEASE ( 11 FDA reports)
FEMUR FRACTURE ( 10 FDA reports)
GAIT DISTURBANCE ( 10 FDA reports)
INFECTION ( 10 FDA reports)
JAUNDICE ( 10 FDA reports)
LIVER DISORDER ( 10 FDA reports)
MUSCULAR WEAKNESS ( 10 FDA reports)
SOMNOLENCE ( 10 FDA reports)
ABDOMINAL PAIN ( 9 FDA reports)
BRADYCARDIA ( 9 FDA reports)
FEELING ABNORMAL ( 9 FDA reports)
HAEMORRHAGE ( 9 FDA reports)
OVERDOSE ( 9 FDA reports)
RASH ( 9 FDA reports)
TREMOR ( 9 FDA reports)
URINARY TRACT INFECTION ( 9 FDA reports)
ABASIA ( 8 FDA reports)
AMNESIA ( 8 FDA reports)
ARTERIOSCLEROSIS OBLITERANS ( 8 FDA reports)
BLOOD PRESSURE INCREASED ( 8 FDA reports)
DRUG INEFFECTIVE ( 8 FDA reports)
DYSLALIA ( 8 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 8 FDA reports)
HALLUCINATION, VISUAL ( 8 FDA reports)
HYPERKALAEMIA ( 8 FDA reports)
PALPITATIONS ( 8 FDA reports)
PNEUMONIA ASPIRATION ( 8 FDA reports)
SKIN ULCER ( 8 FDA reports)
ABDOMINAL PAIN UPPER ( 7 FDA reports)
ABNORMAL BEHAVIOUR ( 7 FDA reports)
ARTERIOSCLEROSIS ( 7 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 7 FDA reports)
CARDIAC FAILURE ( 7 FDA reports)
CARDIAC FAILURE CHRONIC ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DIARRHOEA ( 7 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 7 FDA reports)
HEPATITIS FULMINANT ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
NEPHROTIC SYNDROME ( 7 FDA reports)
PARONYCHIA ( 7 FDA reports)
PLEURAL EFFUSION ( 7 FDA reports)
RESTLESSNESS ( 7 FDA reports)
ANOREXIA ( 6 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 6 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 6 FDA reports)
CONDITION AGGRAVATED ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DELIRIUM ( 6 FDA reports)
DISEASE PROGRESSION ( 6 FDA reports)
DISORIENTATION ( 6 FDA reports)
HAEMODIALYSIS ( 6 FDA reports)
LARYNGEAL OEDEMA ( 6 FDA reports)
MANIA ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
OSTEOMYELITIS ( 6 FDA reports)
RENAL DISORDER ( 6 FDA reports)
STREPTOCOCCAL INFECTION ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
TIBIA FRACTURE ( 6 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 6 FDA reports)
ABDOMINAL DISCOMFORT ( 5 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 5 FDA reports)
AGGRESSION ( 5 FDA reports)
CARDIAC ARREST ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
CHOLESTASIS ( 5 FDA reports)
CONFUSIONAL STATE ( 5 FDA reports)
DERMATITIS ACNEIFORM ( 5 FDA reports)
DERMATITIS EXFOLIATIVE ( 5 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 5 FDA reports)
ENTEROCOLITIS ( 5 FDA reports)
FAECAL INCONTINENCE ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
GASTROENTERITIS ( 5 FDA reports)
HAEMORRHAGE SUBCUTANEOUS ( 5 FDA reports)
HAEMORRHAGIC DIATHESIS ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HEPATITIS ( 5 FDA reports)
HYPERGLYCAEMIA ( 5 FDA reports)
MELAENA ( 5 FDA reports)
MYCOBACTERIUM KANSASII INFECTION ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PRURITUS ( 5 FDA reports)
PSEUDOMONAS INFECTION ( 5 FDA reports)
RESPIRATORY ARREST ( 5 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 5 FDA reports)
SEPSIS ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 5 FDA reports)
VENTRICULAR TACHYCARDIA ( 5 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 5 FDA reports)
WOUND INFECTION ( 5 FDA reports)
ACIDOSIS ( 4 FDA reports)
AGITATION ( 4 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ANAPHYLACTIC SHOCK ( 4 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 4 FDA reports)
ASTHENIA ( 4 FDA reports)
BIPOLAR DISORDER ( 4 FDA reports)
BRADYARRHYTHMIA ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
COLON NEOPLASM ( 4 FDA reports)
COMPLETED SUICIDE ( 4 FDA reports)
DECREASED ACTIVITY ( 4 FDA reports)
DETACHMENT OF RETINAL PIGMENT EPITHELIUM ( 4 FDA reports)
DRUG INTERACTION ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
EMPHYSEMA ( 4 FDA reports)
ERYTHEMA MULTIFORME ( 4 FDA reports)
GASTRITIS ( 4 FDA reports)
HAEMATOCRIT DECREASED ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
HYPOCALCAEMIA ( 4 FDA reports)
HYPONATRAEMIA ( 4 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 4 FDA reports)
LEG AMPUTATION ( 4 FDA reports)
MENTAL DISORDER ( 4 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 4 FDA reports)
RETINAL HAEMORRHAGE ( 4 FDA reports)
SEPTIC SHOCK ( 4 FDA reports)
SEROTONIN SYNDROME ( 4 FDA reports)
SHOCK ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
ACCIDENTAL OVERDOSE ( 3 FDA reports)
ACUTE PULMONARY OEDEMA ( 3 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 3 FDA reports)
ANGINA PECTORIS ( 3 FDA reports)
APHASIA ( 3 FDA reports)
APRAXIA ( 3 FDA reports)
ARRHYTHMIA ( 3 FDA reports)
BLOOD ALDOSTERONE DECREASED ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD POTASSIUM INCREASED ( 3 FDA reports)
BODY TEMPERATURE DECREASED ( 3 FDA reports)
BODY TEMPERATURE INCREASED ( 3 FDA reports)
CAPLAN'S SYNDROME ( 3 FDA reports)
CELL MARKER INCREASED ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CHOLECYSTITIS ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
COAGULATION TIME PROLONGED ( 3 FDA reports)
COLD SWEAT ( 3 FDA reports)
COLLAGEN DISORDER ( 3 FDA reports)
COMMUNICATION DISORDER ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DRUG LEVEL INCREASED ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
EMOTIONAL DISORDER ( 3 FDA reports)
ENDOTRACHEAL INTUBATION ( 3 FDA reports)
EOSINOPHIL COUNT INCREASED ( 3 FDA reports)
EROSIVE OESOPHAGITIS ( 3 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 3 FDA reports)
GASTRIC CANCER ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
HAEMATEMESIS ( 3 FDA reports)
HAEMOLYTIC ANAEMIA ( 3 FDA reports)
HEMIPLEGIA ( 3 FDA reports)
HOT FLUSH ( 3 FDA reports)
HYPERBILIRUBINAEMIA ( 3 FDA reports)
HYPOALDOSTERONISM ( 3 FDA reports)
HYPOMAGNESAEMIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 3 FDA reports)
INFLAMMATION ( 3 FDA reports)
INJURY ( 3 FDA reports)
INTESTINAL ISCHAEMIA ( 3 FDA reports)
INTESTINAL OBSTRUCTION ( 3 FDA reports)
LARGE INTESTINAL ULCER ( 3 FDA reports)
LARGE INTESTINE PERFORATION ( 3 FDA reports)
LOGORRHOEA ( 3 FDA reports)
LOWER GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
METABOLIC ACIDOSIS ( 3 FDA reports)
MOANING ( 3 FDA reports)
MYOCLONUS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PERITONEAL TUBERCULOSIS ( 3 FDA reports)
POLYARTERITIS NODOSA ( 3 FDA reports)
PULMONARY ALVEOLAR HAEMORRHAGE ( 3 FDA reports)
PULMONARY HAEMORRHAGE ( 3 FDA reports)
RENAL TUBULAR DISORDER ( 3 FDA reports)
RENIN DECREASED ( 3 FDA reports)
RHEUMATOID ARTHRITIS ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
STEVENS-JOHNSON SYNDROME ( 3 FDA reports)
SUBDURAL HAEMORRHAGE ( 3 FDA reports)
SUICIDAL IDEATION ( 3 FDA reports)
THROMBOSIS IN DEVICE ( 3 FDA reports)
TONIC CONVULSION ( 3 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 3 FDA reports)
TOXIC SKIN ERUPTION ( 3 FDA reports)
URINARY INCONTINENCE ( 3 FDA reports)
URINE POTASSIUM DECREASED ( 3 FDA reports)
UVEITIS ( 3 FDA reports)
VASCULITIS ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
VITREOUS HAEMORRHAGE ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AFFECT LABILITY ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ANAEMIA HAEMOLYTIC AUTOIMMUNE ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
BLOOD CREATINE INCREASED ( 2 FDA reports)
BLOOD CREATININE DECREASED ( 2 FDA reports)
BLOOD GASES ABNORMAL ( 2 FDA reports)
BLOOD MAGNESIUM INCREASED ( 2 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BLOOD URINE PRESENT ( 2 FDA reports)
BRONCHIOLITIS ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
CARDIO-RESPIRATORY ARREST ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
CERVICAL SPINAL STENOSIS ( 2 FDA reports)
CHEILITIS ( 2 FDA reports)
CHROMATURIA ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COMA ( 2 FDA reports)
COMPRESSION FRACTURE ( 2 FDA reports)
CONCOMITANT DISEASE PROGRESSION ( 2 FDA reports)
CUTANEOUS VASCULITIS ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEMENTIA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIALYSIS ( 2 FDA reports)
DIFFICULTY IN WALKING ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DROOLING ( 2 FDA reports)
DRUG DOSE OMISSION ( 2 FDA reports)
DRUG ERUPTION ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
EPIGLOTTIC OEDEMA ( 2 FDA reports)
EXTENSOR PLANTAR RESPONSE ( 2 FDA reports)
FAECES PALE ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FRACTURE ( 2 FDA reports)
GASTRIC VARICES ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
GLOSSITIS ( 2 FDA reports)
HAEMATOCRIT INCREASED ( 2 FDA reports)
HAEMOGLOBIN INCREASED ( 2 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 2 FDA reports)
HAPTOGLOBIN DECREASED ( 2 FDA reports)
HEPATIC ENZYME INCREASED ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPERREFLEXIA ( 2 FDA reports)
HYPERTENSIVE EMERGENCY ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
HYPOGLYCAEMIC UNCONSCIOUSNESS ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOTONIA ( 2 FDA reports)
ILEUS ( 2 FDA reports)
ILIAC ARTERY OCCLUSION ( 2 FDA reports)
INJECTION SITE INDURATION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INTESTINAL PERFORATION ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
ISCHAEMIC HEPATITIS ( 2 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
LOSS OF CONTROL OF LEGS ( 2 FDA reports)
LOWER LIMB FRACTURE ( 2 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MICROANGIOPATHIC HAEMOLYTIC ANAEMIA ( 2 FDA reports)
MOUTH HAEMORRHAGE ( 2 FDA reports)
MUCOCUTANEOUS RASH ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOGLOBINURIA ( 2 FDA reports)
NASAL CONGESTION ( 2 FDA reports)
NASAL SINUS CANCER ( 2 FDA reports)
NERVOUS SYSTEM DISORDER ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PARKINSON'S DISEASE ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PO2 DECREASED ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PROTEIN URINE PRESENT ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PULMONARY FIBROSIS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RAYNAUD'S PHENOMENON ( 2 FDA reports)
RED BLOOD CELL COUNT INCREASED ( 2 FDA reports)
RED BLOOD CELL SCHISTOCYTES PRESENT ( 2 FDA reports)
REFLEXES ABNORMAL ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
RESPIRATORY ACIDOSIS ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHEUMATOID VASCULITIS ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
SCLERODERMA RENAL CRISIS ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SICK SINUS SYNDROME ( 2 FDA reports)
SINUS ARREST ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SPINAL COLUMN INJURY ( 2 FDA reports)
SPLENOMEGALY ( 2 FDA reports)
STAPHYLOCOCCAL SEPSIS ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
STRIDOR ( 2 FDA reports)
SUDDEN DEATH ( 2 FDA reports)
SWELLING ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
SYSTEMIC SCLEROSIS ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THROMBOTIC MICROANGIOPATHY ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TUBERCULOSIS OF GENITOURINARY SYSTEM ( 2 FDA reports)
TUBULOINTERSTITIAL NEPHRITIS ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VENOUS THROMBOSIS ( 2 FDA reports)
VENTRICULAR FIBRILLATION ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WRIST FRACTURE ( 2 FDA reports)
X-RAY ABNORMAL ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ARTERIAL THROMBOSIS LIMB ( 1 FDA reports)
ASCITES ( 1 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILE DUCT STONE ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CALCIUM INCREASED ( 1 FDA reports)
BLOOD CHLORIDE DECREASED ( 1 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BRAIN DEATH ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
CAPILLARY PERMEABILITY INCREASED ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CASTLEMAN'S DISEASE ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CEREBRAL HAEMATOMA ( 1 FDA reports)
CEREBROVASCULAR DISORDER ( 1 FDA reports)
CHOKING SENSATION ( 1 FDA reports)
CHOLANGITIS ACUTE ( 1 FDA reports)
CONJUNCTIVAL OEDEMA ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
COOMBS TEST POSITIVE ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
DENTAL FISTULA ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULUM INTESTINAL HAEMORRHAGIC ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 1 FDA reports)
DRUG-INDUCED LIVER INJURY ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENTEROVESICAL FISTULA ( 1 FDA reports)
EOSINOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
FAT EMBOLISM ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GLYCOSYLATED HAEMOGLOBIN INCREASED ( 1 FDA reports)
GYNAECOMASTIA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATOCELLULAR DAMAGE ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOCOMPLEMENTAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IMMUNOSUPPRESSION ( 1 FDA reports)
IN-STENT CORONARY ARTERY RESTENOSIS ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIPOMA OF BREAST ( 1 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MONOCYTE COUNT INCREASED ( 1 FDA reports)
MONONEUROPATHY MULTIPLEX ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
N-TERMINAL PROHORMONE BRAIN NATRIURETIC PEPTIDE ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHRITIC SYNDROME ( 1 FDA reports)
NERVE INJURY ( 1 FDA reports)
NEUTROPHIL PERCENTAGE INCREASED ( 1 FDA reports)
OCCULT BLOOD ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
ON AND OFF PHENOMENON ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEONECROSIS OF JAW ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ACUTE ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA PNEUMOCOCCAL ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PSEUDOMEMBRANOUS COLITIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
QUADRIPLEGIA ( 1 FDA reports)
RECTAL ULCER HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
STENOTROPHOMONAS INFECTION ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
SUBDURAL HAEMATOMA ( 1 FDA reports)
SURGERY ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TOE AMPUTATION ( 1 FDA reports)
TOOTH EXTRACTION ( 1 FDA reports)
TRANSAMINASES INCREASED ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VISUAL FIELD DEFECT ( 1 FDA reports)
WATER INTOXICATION ( 1 FDA reports)
WOUND ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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