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UNRESPONSIVE TO STIMULI ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MENTAL STATUS CHANGES ( 3 FDA reports)
DRY EYE ( 3 FDA reports)
DEHYDRATION ( 3 FDA reports)
VOMITING ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
MULTIPLE DRUG OVERDOSE ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
FALL ( 2 FDA reports)
DYSSTASIA ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
CEREBRAL HAEMORRHAGE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
CATAPLEXY ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
BREAST CANCER METASTATIC ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEUROGENIC BLADDER ( 1 FDA reports)
NIGHT SWEATS ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL DISCOMFORT ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
POST PROCEDURAL PULMONARY EMBOLISM ( 1 FDA reports)
APNOEA ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SJOGREN'S SYNDROME ( 1 FDA reports)
SPINAL FRACTURE ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TOOTH INFECTION ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
ACCIDENTAL DEATH ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND ( 1 FDA reports)

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