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

VOMITING ( 10 FDA reports)
RENAL FAILURE ( 6 FDA reports)
HYPERSPLENISM ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
STEVENS-JOHNSON SYNDROME ( 5 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 5 FDA reports)
BLOOD TEST ABNORMAL ( 4 FDA reports)
INTESTINAL OBSTRUCTION ( 4 FDA reports)
PANCYTOPENIA ( 4 FDA reports)
PNEUMATOSIS INTESTINALIS ( 4 FDA reports)
PRURITUS ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BONE CYST ( 3 FDA reports)
DYSPNOEA ( 3 FDA reports)
HEPATIC NEOPLASM MALIGNANT ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
PSORIASIS ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
APPLICATION SITE VESICLES ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ATAXIA ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
COUGH ( 2 FDA reports)
DEMENTIA ALZHEIMER'S TYPE ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DERMATITIS ATOPIC ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
ERYTHEMA ( 2 FDA reports)
FEBRILE NEUTROPENIA ( 2 FDA reports)
FEELING HOT ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GASTRIC MUCOSA ERYTHEMA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
LYMPHOPENIA ( 2 FDA reports)
MIOSIS ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OTITIS MEDIA ( 2 FDA reports)
PNEUMOPERITONEUM ( 2 FDA reports)
PORTAL HYPERTENSIVE GASTROPATHY ( 2 FDA reports)
PULMONARY HAEMORRHAGE ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
RADIUS FRACTURE ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
ULNA FRACTURE ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
ACIDOSIS ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAEMIA MACROCYTIC ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASTHMA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALBUMIN DECREASED ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BILIRUBIN INCREASED ( 1 FDA reports)
BLOOD CORTISOL DECREASED ( 1 FDA reports)
BLOOD URIC ACID ABNORMAL ( 1 FDA reports)
BOWEN'S DISEASE ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CARCINOMA ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONJUNCTIVITIS ( 1 FDA reports)
CRANIAL NERVE DISORDER ( 1 FDA reports)
CUSHING'S SYNDROME ( 1 FDA reports)
CYTOLYTIC HEPATITIS ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECUBITUS ULCER ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FATIGUE ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART VALVE REPLACEMENT ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HEPATIC NEOPLASM ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYDROPNEUMOTHORAX ( 1 FDA reports)
HYPEREOSINOPHILIC SYNDROME ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOPITUITARISM ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PIRIFORMIS SYNDROME ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PROTEIN TOTAL DECREASED ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SINUS TACHYCARDIA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THYROXINE DECREASED ( 1 FDA reports)
TRAUMATIC LUNG INJURY ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE COLOUR ABNORMAL ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VENTRICULAR ARRHYTHMIA ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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