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

WEIGHT INCREASED ( 4 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
ABSCESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
VOMITING ( 2 FDA reports)
BLOOD CORTISOL DECREASED ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE INFARCTION ( 2 FDA reports)
BONE PAIN ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
DISORIENTATION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INEFFECTIVE ( 2 FDA reports)
ENCEPHALITIS ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
TREMOR ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
SKIN DISCOLOURATION ( 2 FDA reports)
SEASONAL ALLERGY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
MENINGITIS VIRAL ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
MENINGITIS ASEPTIC ( 2 FDA reports)
MEMORY IMPAIRMENT ( 2 FDA reports)
MALAISE ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
IMPAIRED DRIVING ABILITY ( 2 FDA reports)
INFECTION ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
HYPOREFLEXIA ( 1 FDA reports)
HYPERTROPHY ( 1 FDA reports)
MENINGEAL DISORDER ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MULTI-ORGAN FAILURE ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
GLASGOW COMA SCALE ABNORMAL ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ORGAN FAILURE ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
FOOD INTERACTION ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
FACE OEDEMA ( 1 FDA reports)
ESCHERICHIA INFECTION ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
ENCEPHALITIS VIRAL ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
ANURIA ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)

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