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

FALL ( 5 FDA reports)
DRUG EFFECT DECREASED ( 4 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
INSOMNIA ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
RIB FRACTURE ( 2 FDA reports)
AGRANULOCYTOSIS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
ALCOHOL POISONING ( 2 FDA reports)
ORAL INTAKE REDUCED ( 2 FDA reports)
ANAL ABSCESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LUMBAR VERTEBRAL FRACTURE ( 2 FDA reports)
BACK INJURY ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BONE MARROW DISORDER ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
COUGH ( 1 FDA reports)
CYSTITIS GLANDULARIS ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
EPIDIDYMITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOGLOBINURIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LDL/HDL RATIO ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
MYELODYSPLASTIC SYNDROME ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
ANAESTHETIC COMPLICATION NEUROLOGICAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PERIANAL ABSCESS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PROCEDURAL HYPERTENSION ( 1 FDA reports)
PROCEDURAL PAIN ( 1 FDA reports)
PROPHYLAXIS ( 1 FDA reports)
PROSTATIC MASS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)

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