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

FLUSHING ( 9 FDA reports)
PRURITUS ( 5 FDA reports)
DRUG INEFFECTIVE ( 5 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 4 FDA reports)
DIARRHOEA ( 4 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
PNEUMONIA BACTERIAL ( 3 FDA reports)
PARAESTHESIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
LUNG NEOPLASM ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
GASTROINTESTINAL INFLAMMATION ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
DIZZINESS ( 3 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
VOMITING ( 2 FDA reports)
SMALL INTESTINAL OBSTRUCTION ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
COUGH ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
FOREIGN BODY ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTRIC HAEMORRHAGE ( 1 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
CHILLS ( 1 FDA reports)
FALL ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
HEADACHE ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTENTIONAL DRUG MISUSE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
DEATH ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 1 FDA reports)
MALAISE ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
PAIN ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
PERIPHERAL EMBOLISM ( 1 FDA reports)
ERECTILE DYSFUNCTION ( 1 FDA reports)
PRODUCT ADHESION ISSUE ( 1 FDA reports)
PRODUCT QUALITY ISSUE ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
DYSPNOEA EXACERBATED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
DRUG INTERACTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)

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