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
8016606 8286190 F 8016606-7 20111230 20111231 EXP GB-ACCORD-011469 ACCORDHCP 35 YR F Y 20111231 OT UNITED KINGDOM

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
8016606 1018419863 PS FINASTERIDE 1 090121
8016606 1018419864 C FOLIC ACID 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
8016606 1018419863 PRODUCT USED FOR UNKNOWN INDICATION

Outcome of event

Event ID OUTC COD
8016606 OT

Reactions reported

Event ID PT
8016606 MATERNAL EXPOSURE DURING PREGNANCY
8016606 ACCIDENTAL EXPOSURE
8016606 NO ADVERSE EVENT
8016606 WRONG TECHNIQUE IN DRUG USAGE PROCESS

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found