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
7386768 6970828 F 7386768-3 20090228 20110324 20110331 EXP FR-ASTRAZENECA-2009CG00658 AZPRODUW00 25579 DY M Y 100 KG 20110331 MD 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
7386768 1016138907 C EFFEXOR 1 ORAL
7386768 1016138908 C IMOVANE 2 ORAL
7386768 1016138909 C DECAPEPTYL 2 SUBCUTANEOUS
7386768 1016138905 SS VANDETANIB 2 ORAL
7386768 1016138906 C PREVISCAN 2 ORAL
7386768 1016138904 PS CASODEX 1 ORAL 020498

Indications of drugs used

Event ID DRUG SEQ INDI PT
7386768 1016138907 DEPRESSION
7386768 1016138908 INSOMNIA
7386768 1016138909 PROSTATE CANCER
7386768 1016138905 PROSTATE CANCER METASTATIC
7386768 1016138906 THROMBOSIS PROPHYLAXIS
7386768 1016138904 PROSTATE CANCER METASTATIC

Outcome of event

Event ID OUTC COD
7386768 HO

Reactions reported

Event ID PT
7386768 PHOTOSENSITIVITY REACTION

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
7386768 1016138905 20090110 20090406 87 DAY
7386768 1016138904 20090110 20090406 87 DAY