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

CONVULSION ( 24 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 18 FDA reports)
FATIGUE ( 18 FDA reports)
HAEMOGLOBIN DECREASED ( 18 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 17 FDA reports)
HAEMOLYSIS ( 17 FDA reports)
CONFUSIONAL STATE ( 15 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 14 FDA reports)
BLOOD CREATININE INCREASED ( 14 FDA reports)
BLOOD GLUCOSE INCREASED ( 14 FDA reports)
COMA URAEMIC ( 14 FDA reports)
DISTURBANCE IN ATTENTION ( 14 FDA reports)
GASTROINTESTINAL DISORDER ( 14 FDA reports)
GRAND MAL CONVULSION ( 14 FDA reports)
HAEMOLYTIC URAEMIC SYNDROME ( 14 FDA reports)
LYMPHOCYTE COUNT DECREASED ( 14 FDA reports)
THROMBOCYTOPENIA ( 14 FDA reports)
ESCHERICHIA TEST POSITIVE ( 13 FDA reports)
ANISOCYTOSIS ( 12 FDA reports)
ASTHENIA ( 12 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 12 FDA reports)
BLOOD UREA INCREASED ( 12 FDA reports)
BLOOD URIC ACID DECREASED ( 12 FDA reports)
CANDIDIASIS ( 12 FDA reports)
PYREXIA ( 12 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 10 FDA reports)
PULMONARY OEDEMA ( 10 FDA reports)
HYPERGLYCAEMIA ( 9 FDA reports)
PAIN IN EXTREMITY ( 9 FDA reports)
ESCHERICHIA URINARY TRACT INFECTION ( 8 FDA reports)
MYOCARDITIS ( 8 FDA reports)
RENAL FAILURE ( 8 FDA reports)
URINARY TRACT INFECTION ( 8 FDA reports)
DIZZINESS ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
NAUSEA ( 7 FDA reports)
VOMITING ( 7 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DIARRHOEA ( 6 FDA reports)
ESCHERICHIA BACTERAEMIA ( 6 FDA reports)
HYPOKALAEMIA ( 6 FDA reports)
MUSCULAR WEAKNESS ( 6 FDA reports)
RENAL FAILURE ACUTE ( 6 FDA reports)
SINUS TACHYCARDIA ( 6 FDA reports)
FALL ( 5 FDA reports)
HAEMATURIA ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
INFECTION ( 5 FDA reports)
TREMOR ( 5 FDA reports)
ACUTE RESPIRATORY FAILURE ( 4 FDA reports)
BREATH SOUNDS ABNORMAL ( 4 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
CHEST X-RAY ABNORMAL ( 4 FDA reports)
DEATH ( 4 FDA reports)
EJECTION FRACTION DECREASED ( 4 FDA reports)
EYE PAIN ( 4 FDA reports)
HAEMOLYTIC ANAEMIA ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
HYPERHIDROSIS ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTHERMIA ( 4 FDA reports)
HYPOKINESIA ( 4 FDA reports)
INFLUENZA LIKE ILLNESS ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MITRAL VALVE INCOMPETENCE ( 4 FDA reports)
NEPHROLITHIASIS ( 4 FDA reports)
PERICARDIAL EFFUSION ( 4 FDA reports)
PROLONGED EXPIRATION ( 4 FDA reports)
RESPIRATORY DISORDER ( 4 FDA reports)
APHASIA ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
COMA ( 3 FDA reports)
CONTUSION ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
HEART RATE DECREASED ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
NYSTAGMUS ( 3 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
BLADDER SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 2 FDA reports)
BLOOD CALCIUM INCREASED ( 2 FDA reports)
BLOOD CHLORIDE DECREASED ( 2 FDA reports)
BLOOD PH INCREASED ( 2 FDA reports)
BLOOD POTASSIUM INCREASED ( 2 FDA reports)
BLOOD SODIUM DECREASED ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CLOSTRIDIAL INFECTION ( 2 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 2 FDA reports)
COUGH ( 2 FDA reports)
DECREASED IMMUNE RESPONSIVENESS ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ENCEPHALOPATHY ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HEAT RASH ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPOAESTHESIA ( 2 FDA reports)
INFUSION RELATED REACTION ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
LIVER DISORDER ( 2 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 2 FDA reports)
LYMPHOCYTE PERCENTAGE DECREASED ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
NEUROGENIC BLADDER ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PCO2 DECREASED ( 2 FDA reports)
PLATELET COUNT INCREASED ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PO2 INCREASED ( 2 FDA reports)
POST PROCEDURAL NAUSEA ( 2 FDA reports)
POST PROCEDURAL VOMITING ( 2 FDA reports)
POSTOPERATIVE ILEUS ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
RASH ( 2 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 2 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 2 FDA reports)
SALIVARY GLAND ENLARGEMENT ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THROAT IRRITATION ( 2 FDA reports)
URGE INCONTINENCE ( 2 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 2 FDA reports)
URINARY TRACT INFECTION FUNGAL ( 2 FDA reports)
VITAMIN B12 DEFICIENCY ( 2 FDA reports)
VITAMIN D DEFICIENCY ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALBUMIN URINE ( 1 FDA reports)
ALBUMIN URINE PRESENT ( 1 FDA reports)
ALBUMINURIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
APPENDICITIS ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATROPHIC VULVOVAGINITIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BASOPHIL PERCENTAGE DECREASED ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD BICARBONATE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD PHOSPHORUS INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DIASTOLIC DECREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CEREBRAL ATROPHY ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CLAVICLE FRACTURE ( 1 FDA reports)
CLOSTRIDIUM COLITIS ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CREATINE URINE DECREASED ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
IMMUNODEFICIENCY COMMON VARIABLE ( 1 FDA reports)
IMMUNOGLOBULINS DECREASED ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INADEQUATE ANALGESIA ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
JAUNDICE ( 1 FDA reports)
LUNG INFILTRATION ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGITIS ( 1 FDA reports)
MENINGITIS ASEPTIC ( 1 FDA reports)
METASTASES TO LUNG ( 1 FDA reports)
METASTASES TO SPINE ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
NITRITE URINE PRESENT ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PLATELET DISORDER ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PROGRESSIVE MULTIPLE SCLEROSIS ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TENSION ( 1 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND COMPLICATION ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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