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

UNINTENDED PREGNANCY ( 8 FDA reports)
INCORRECT DOSE ADMINISTERED ( 7 FDA reports)
ACCIDENTAL EXPOSURE ( 6 FDA reports)
RASH ( 5 FDA reports)
INJECTION SITE PAIN ( 4 FDA reports)
INJECTION SITE BURNING ( 3 FDA reports)
CROHN'S DISEASE ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
MALAISE ( 2 FDA reports)
LARGE INTESTINAL HAEMORRHAGE ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
GASTROINTESTINAL PAIN ( 2 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 2 FDA reports)
DEFAECATION URGENCY ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 2 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
CYSTITIS ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
COUGH ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INJECTION SITE IRRITATION ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INJECTION SITE SCAR ( 1 FDA reports)
INJECTION SITE URTICARIA ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
INTERVERTEBRAL DISC DISORDER ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOOSE STOOLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
MATERNAL EXPOSURE DURING DELIVERY ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MYELITIS ( 1 FDA reports)
CHILLS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NEUROLOGICAL SYMPTOM ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STREPTOCOCCAL INFECTION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use