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
5526849 6448638 F 5526849-X 20070820 20071119 20071127 EXP BE-ASTRAZENECA-2007AC01886 AZPRODUW00 25120 DY M Y 20071127 MD BELGIUM

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
5526849 1009197954 PS CRESTOR 1 ORAL 021366
5526849 1009197955 C AMLOR 2
5526849 1009197956 C PERSANTINE 1 PERSANTINE 75

Indications of drugs used

no results found

Outcome of event

Event ID OUTC COD
5526849 DS
5526849 OT

Reactions reported

Event ID PT
5526849 ARTHRALGIA
5526849 BRADYCARDIA
5526849 FATIGUE
5526849 MUSCLE SPASMS
5526849 MUSCLE SWELLING
5526849 MYALGIA

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
5526849 1009197954 20070712 20071001 82 DAY
5526849 1009197955 20030101
5526849 1009197956 20040101