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
7059599 7631858 F 7059599-1 20090101 20101015 20101025 EXP CN-ASTRAZENECA-2010SE47636 AZPRODUW00 5 YR Y 20101025 MD CHINA

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
7059599 1014957462 C NASONEX 1 NASAL
7059599 1014957460 PS PULMICORT 1 RESPIRATORY (INHALATION) 020441
7059599 1014957461 SS FLUTICASONE PROPIONATE 1 RESPIRATORY (INHALATION) 125-250 UG DAILY

Indications of drugs used

Event ID DRUG SEQ INDI PT
7059599 1014957462 RHINITIS
7059599 1014957460 ASTHMA
7059599 1014957461 ASTHMA

Outcome of event

Event ID OUTC COD
7059599 OT

Reactions reported

Event ID PT
7059599 PAIN IN EXTREMITY
7059599 OSTEONECROSIS

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
7059599 1014957460 20071201 20100401 28 MON
7059599 1014957461 20100401 20100901 5 MON