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

HYPERHIDROSIS ( 11 FDA reports)
WEIGHT INCREASED ( 9 FDA reports)
FATIGUE ( 9 FDA reports)
BACK PAIN ( 8 FDA reports)
BREAST ENLARGEMENT ( 7 FDA reports)
CARDIAC DISORDER ( 7 FDA reports)
GAIT DISTURBANCE ( 7 FDA reports)
URINE OUTPUT DECREASED ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
WITHDRAWAL SYNDROME ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
DYSTONIA ( 7 FDA reports)
DYSPNOEA ( 7 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 4 FDA reports)
PAIN ( 4 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 4 FDA reports)
AMNESIA ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
OESOPHAGEAL RUPTURE ( 2 FDA reports)
RESORPTION BONE INCREASED ( 2 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR INFECTION VIRAL ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
FAECES HARD ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MASS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPPORTUNISTIC INFECTION ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
CYTOMEGALOVIRUS INFECTION ( 1 FDA reports)
COUGH ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)

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