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

RASH ( 8 FDA reports)
DRUG INEFFECTIVE ( 6 FDA reports)
DYSPNOEA ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
ASTHMA ( 4 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 4 FDA reports)
EXANTHEM ( 4 FDA reports)
TONSILLITIS ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
MALAISE ( 3 FDA reports)
OESOPHAGEAL ULCER ( 3 FDA reports)
BRAIN NEOPLASM ( 2 FDA reports)
BRONCHIAL OEDEMA ( 2 FDA reports)
CARDIAC ARREST ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
ERYTHEMA MULTIFORME ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOOD INTOLERANCE ( 2 FDA reports)
HEPATITIS CHOLESTATIC ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
MERYCISM ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
ODYNOPHAGIA ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
OESOPHAGEAL INJURY ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
REGURGITATION ( 2 FDA reports)
RENAL FAILURE CHRONIC ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFLAMMATION ( 2 FDA reports)
VAGINAL EROSION ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BLOOD CREATININE ABNORMAL ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CHRONIC MYELOID LEUKAEMIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FALSE POSITIVE LABORATORY RESULT ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERKALAEMIA ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTRA-UTERINE DEATH ( 1 FDA reports)
LYMPHOCYTE STIMULATION TEST POSITIVE ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL MUCOSAL DISSECTION ( 1 FDA reports)
ORAL DISORDER ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
POOR PERIPHERAL CIRCULATION ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT PACKAGING QUANTITY ISSUE ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)

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