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
5526852 6475483 I 5526852-X 20070101 20071120 20071127 EXP FR-ASTRAZENECA-2007CG01641 AZPRODUW00 781 MON M Y 20071127 OT FRANCE

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
5526852 1009197960 PS CRESTOR 1 ORAL 21366
5526852 1009197961 SS CRESTOR 1 ORAL 021366
5526852 1009197962 SS ELISOR 2 ORAL
5526852 1009197963 C MOPRAL 2 ORAL
5526852 1009197964 C KIVEXA 2 ORAL
5526852 1009197965 C TELZIR 1
5526852 1009197966 C NORVIR 1
5526852 1009197967 C LASIX 1
5526852 1009197968 C XATRAL 2
5526852 1009197969 C PLAVIX 1
5526852 1009197970 C SECTRAL 1
5526852 1009197971 C TANAKAN 2
5526852 1009197972 C LEXOMIL 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5526852 1009197960 DYSLIPIDAEMIA

Outcome of event

Event ID OUTC COD
5526852 HO

Reactions reported

Event ID PT
5526852 CEREBELLAR ATAXIA
5526852 CONDITION AGGRAVATED
5526852 NEURALGIA

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
5526852 1009197960 20061128 20070626 211 DAY
5526852 1009197961 20070626 20071011 108 DAY
5526852 1009197962 20061128
5526852 1009197964 20070601