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KAPOSI'S VARICELLIFORM ERUPTION ( 5 FDA reports)
APPLICATION SITE WARMTH ( 4 FDA reports)
ACTINIC KERATOSIS ( 2 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 2 FDA reports)
SQUAMOUS CELL CARCINOMA ( 2 FDA reports)
SCAR ( 2 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 2 FDA reports)
INFECTED EPIDERMAL CYST ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
EOSINOPHIL COUNT INCREASED ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
CARDIAC FAILURE ACUTE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CHEST PAIN ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
ENTEROCOCCAL INFECTION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
EOSINOPHILIC PNEUMONIA ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEPATOMEGALY ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
B-CELL LYMPHOMA ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJURY ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MANIA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MUCORMYCOSIS ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PERSECUTORY DELUSION ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA CYTOMEGALOVIRAL ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PULMONARY HAEMORRHAGE ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY INFARCTION ( 1 FDA reports)
RASH ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL ARTERY STENOSIS ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESUSCITATION ( 1 FDA reports)
RETCHING ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
APPLICATION SITE INFECTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUSITIS FUNGAL ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SMALL CELL CARCINOMA ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDE ATTEMPT ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)

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