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

DYSURIA ( 7 FDA reports)
DEHYDRATION ( 6 FDA reports)
DIZZINESS ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
CONSTIPATION ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
VISION BLURRED ( 5 FDA reports)
HEADACHE ( 4 FDA reports)
PAIN ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
ALPHA HAEMOLYTIC STREPTOCOCCAL INFECTION ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BACTERIAL SEPSIS ( 3 FDA reports)
COORDINATION ABNORMAL ( 3 FDA reports)
COUGH ( 3 FDA reports)
DEPRESSED MOOD ( 3 FDA reports)
DRUG INEFFECTIVE ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
MEMORY IMPAIRMENT ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
ORTHOSTATIC HYPOTENSION ( 3 FDA reports)
PLEURAL EFFUSION ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
THOUGHT BLOCKING ( 3 FDA reports)
VOMITING ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ATELECTASIS ( 2 FDA reports)
BACTERAEMIA ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CRYING ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
ELECTROCARDIOGRAM QRS COMPLEX ABNORMAL ( 2 FDA reports)
FALL ( 2 FDA reports)
GENERALISED OEDEMA ( 2 FDA reports)
HYDRONEPHROSIS ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
LEUKOCYTOSIS ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LUNG INFILTRATION ( 2 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 2 FDA reports)
MANIA ( 2 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPIRATION PLEURAL CAVITY ABNORMAL ( 1 FDA reports)
BACTERIA STOOL IDENTIFIED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
CATHETER RELATED INFECTION ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COAGULOPATHY ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
GASTRITIS ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
LYMPHOMA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA REFRACTORY ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OPTIC NEURITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SERUM FERRITIN INCREASED ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use