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

DIZZINESS ( 9 FDA reports)
ASTHENIA ( 6 FDA reports)
BACK PAIN ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
FEMUR FRACTURE ( 6 FDA reports)
CORONARY ARTERY DISEASE ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
CELLULITIS ( 4 FDA reports)
CEREBROVASCULAR ACCIDENT ( 4 FDA reports)
FALL ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PNEUMONIA ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
ABDOMINAL ABSCESS ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
CARDIOGENIC SHOCK ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CELLULITIS STAPHYLOCOCCAL ( 2 FDA reports)
CHOLECYSTITIS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CORONARY ARTERY BYPASS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DIVERTICULUM INTESTINAL ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EYE HAEMORRHAGE ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
MACULAR DEGENERATION ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
MYOCARDIAL INFARCTION ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
PAIN ( 2 FDA reports)
PERFORATION BILE DUCT ( 2 FDA reports)
PERITONEAL INFECTION ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RASH ( 2 FDA reports)
RASH PRURITIC ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
THROMBOCYTOPENIA ( 2 FDA reports)
TOXIC SHOCK SYNDROME ( 2 FDA reports)
TRANSPLANT REJECTION ( 2 FDA reports)
URTICARIA ( 2 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGRANULOCYTOSIS ( 1 FDA reports)
ALLERGY TO PLANTS ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BILE DUCT OBSTRUCTION ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
CANDIDA PNEUMONIA ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
EPILEPSY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EPSTEIN-BARR VIRUS ASSOCIATED LYMPHOPROLIFERATIVE DISORDER ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEEDING DISORDER ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
GRANULOCYTOPENIA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HEMIPARESIS ( 1 FDA reports)
HEPATIC CIRRHOSIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HEPATITIS CHOLESTATIC ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTHERMIA ( 1 FDA reports)
HYPERVENTILATION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTESTINAL CYST ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS TUBERCULOUS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYOPATHY TOXIC ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
NEUROTOXICITY ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NEUTROPHIL COUNT DECREASED ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
OCULOMUCOCUTANEOUS SYNDROME ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
POSTOPERATIVE WOUND INFECTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
READING DISORDER ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
RETINAL PIGMENT EPITHELIAL TEAR ( 1 FDA reports)
RHABDOMYOLYSIS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SKELETAL INJURY ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STAPHYLOCOCCAL SKIN INFECTION ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDONITIS ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)

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