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
5903220 6682529 F 5903220-X 20080926 20080930 EXP A0698987A GLAXOSMITHKLINE 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
5903220 1010519802 PS ALLI 1 ORAL UNK 021887

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5903220 OT

Reactions reported

Event ID PT
5903220 BACK INJURY
5903220 CONSTIPATION
5903220 DRUG INEFFECTIVE
5903220 DYSPHAGIA
5903220 DYSPNOEA
5903220 DYSPNOEA EXERTIONAL
5903220 FATIGUE
5903220 FOOD CRAVING
5903220 GAIT DISTURBANCE
5903220 GASTROINTESTINAL DISORDER
5903220 HYPERPHAGIA
5903220 HYPERSENSITIVITY
5903220 HYPOTHYROIDISM
5903220 OROPHARYNGEAL PAIN
5903220 PAIN
5903220 RECTAL DISCHARGE
5903220 STEATORRHOEA
5903220 SWELLING
5903220 SWOLLEN TONGUE
5903220 THERAPEUTIC RESPONSE UNEXPECTED
5903220 THROAT TIGHTNESS
5903220 THYROIDITIS
5903220 WEIGHT FLUCTUATION
5903220 WEIGHT INCREASED

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
5903220 1010519802 20071101