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

DRUG INEFFECTIVE ( 32 FDA reports)
SOMNOLENCE ( 8 FDA reports)
URTICARIA ( 7 FDA reports)
HYPERSENSITIVITY ( 7 FDA reports)
NAUSEA ( 6 FDA reports)
FATIGUE ( 6 FDA reports)
INSOMNIA ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
SWOLLEN TONGUE ( 4 FDA reports)
RASH PRURITIC ( 4 FDA reports)
LIP SWELLING ( 4 FDA reports)
ABASIA ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
GENERAL PHYSICAL CONDITION ABNORMAL ( 3 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
EMPHYSEMA ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
HOMICIDE ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
HANGOVER ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NASAL OEDEMA ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIGHTMARE ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN ( 1 FDA reports)
COUGH ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
REBOUND EFFECT ( 1 FDA reports)
RENAL PAIN ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
ALCOHOL INTERACTION ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
ACCIDENT ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
TREMOR ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)

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