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

DYSPNOEA ( 11 FDA reports)
FATIGUE ( 11 FDA reports)
LEUKOPENIA ( 6 FDA reports)
THROMBOCYTOPENIA ( 6 FDA reports)
ANAEMIA ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
DELIRIUM ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
WEIGHT DECREASED ( 5 FDA reports)
CARDIAC FAILURE ( 4 FDA reports)
DEMENTIA ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
EPILEPSY ( 4 FDA reports)
MUSCLE SPASMS ( 4 FDA reports)
MYALGIA ( 4 FDA reports)
PALPITATIONS ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VOMITING ( 4 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
CARDIAC ASTHMA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
CIRCULATORY COLLAPSE ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
COUGH ( 3 FDA reports)
DECUBITUS ULCER ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
FALL ( 3 FDA reports)
FLATULENCE ( 3 FDA reports)
HALLUCINATION ( 3 FDA reports)
HYPERHIDROSIS ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
HYPOTENSION ( 3 FDA reports)
OESOPHAGITIS ( 3 FDA reports)
PAIN ( 3 FDA reports)
RENAL FAILURE ( 3 FDA reports)
RENAL IMPAIRMENT ( 3 FDA reports)
TREMOR ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANGINA UNSTABLE ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTERIAL FIBROSIS ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLADDER CATHETERISATION ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
COGNITIVE DETERIORATION ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
CRANIAL NERVE INFECTION ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DRUG LEVEL INCREASED ( 2 FDA reports)
DYSARTHRIA ( 2 FDA reports)
FLUID RETENTION ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 2 FDA reports)
HYPERVENTILATION ( 2 FDA reports)
HYPOCALCAEMIA ( 2 FDA reports)
INCONTINENCE ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INFLUENZA LIKE ILLNESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MYELODYSPLASTIC SYNDROME ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
ORTHOPNOEA ( 2 FDA reports)
ORTHOSTATIC HYPOTENSION ( 2 FDA reports)
OSTEONECROSIS ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PANCYTOPENIA ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
RENAL FAILURE ACUTE ( 2 FDA reports)
RHINITIS ( 2 FDA reports)
SEPSIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
WEIGHT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE MARROW DEPRESSION ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
ESCHERICHIA SEPSIS ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMOLYTIC ANAEMIA ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOTHERMIA ( 1 FDA reports)
HYPOVENTILATION ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LUNG CARCINOMA CELL TYPE UNSPECIFIED RECURRENT ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
OCULAR ICTERUS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PARKINSONISM ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
SENSATION OF HEAVINESS ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SUDDEN CARDIAC DEATH ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TYPE IV HYPERSENSITIVITY REACTION ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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