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DRUG INEFFECTIVE ( 6 FDA reports)
DRUG EFFECT DECREASED ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
CROHN'S DISEASE ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
HEADACHE ( 4 FDA reports)
MEDICATION RESIDUE ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
PRODUCT QUALITY ISSUE ( 3 FDA reports)
DIVERTICULITIS ( 3 FDA reports)
FEMALE GENITAL TRACT FISTULA ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
SNEEZING ( 2 FDA reports)
SINUS HEADACHE ( 2 FDA reports)
SINUS DISORDER ( 2 FDA reports)
SENSATION OF PRESSURE ( 2 FDA reports)
SCAB ( 2 FDA reports)
RECTAL ADENOMA ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
PULMONARY EMBOLISM ( 2 FDA reports)
PRODUCT ODOUR ABNORMAL ( 2 FDA reports)
DRUG INTERACTION ( 2 FDA reports)
PREMATURE LABOUR ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
PAIN ( 2 FDA reports)
NASAL DISORDER ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTRA-UTERINE DEATH ( 2 FDA reports)
LUNG ABSCESS ( 2 FDA reports)
MALAISE ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
LARYNGEAL CYST ( 1 FDA reports)
INJECTION SITE NECROSIS ( 1 FDA reports)
NAUSEA ( 1 FDA reports)
NECROSIS ISCHAEMIC ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGEAL SPASM ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
HYPERBILIRUBINAEMIA NEONATAL ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PREMATURE BABY ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ALCOHOLISM ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)

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