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

PAIN IN EXTREMITY ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
NEUTROPHILIA ( 2 FDA reports)
NAUSEA ( 2 FDA reports)
ARTERIAL STENT INSERTION ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
MALAISE ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
INJECTION SITE IRRITATION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GAIT DISTURBANCE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
CATHETERISATION CARDIAC ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
CHRONIC OBSTRUCTIVE AIRWAYS DISEASE EXACERBATED ( 2 FDA reports)
DYSPEPSIA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
CRYING ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
CACHEXIA ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAIR COLOUR CHANGES ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
KERATITIS SCLEROSING ( 1 FDA reports)
ATOPY ( 1 FDA reports)
LYMPHADENOPATHY ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
ARTHRALGIA ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NAIL INFECTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
PAIN ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PCO2 DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PYOGENIC GRANULOMA ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
TEARFULNESS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WEIGHT INCREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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