The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5903219 6467750 F 5903219-3 20070701 20080926 20080930 EXP A0680111A GLAXOSMITHKLINE 41 YR F Y 20080930 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5903219 1010519800 PS ALLI 1 ORAL UNK 21887
5903219 1010519801 SS UNSPECIFIED MEDICATION 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5903219 1010519800 WEIGHT LOSS DIET

Outcome of event

Event ID OUTC COD
5903219 OT

Reactions reported

Event ID PT
5903219 ABDOMINAL PAIN UPPER
5903219 ABNORMAL FAECES
5903219 BLINDNESS
5903219 CONTUSION
5903219 DECREASED APPETITE
5903219 DIARRHOEA
5903219 DISCOMFORT
5903219 DISTURBANCE IN ATTENTION
5903219 DRUG INEFFECTIVE
5903219 DRY MOUTH
5903219 EATING DISORDER
5903219 FAECAL INCONTINENCE
5903219 FATIGUE
5903219 FLATULENCE
5903219 FLUID RETENTION
5903219 FRUSTRATION
5903219 GASTROINTESTINAL DISORDER
5903219 HEADACHE
5903219 HUNGER
5903219 HYPERPHAGIA
5903219 ILL-DEFINED DISORDER
5903219 MALAISE
5903219 MENTAL IMPAIRMENT
5903219 MIGRAINE
5903219 MUSCULOSKELETAL STIFFNESS
5903219 NASOPHARYNGITIS
5903219 OROPHARYNGEAL PAIN
5903219 PAIN
5903219 RECTAL DISCHARGE
5903219 STEATORRHOEA
5903219 THIRST
5903219 WEIGHT FLUCTUATION
5903219 WEIGHT INCREASED
5903219 WISDOM TEETH REMOVAL

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5903219 1010519800 20070801 20080617