The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
125926611 12592661 1 I 201604 20160718 20160726 20160726 EXP US-009507513-1607USA007542 MERCK 35.00 YR F Y 106.58000 KG 20160726 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
125926611 12592661 1 PS IMPLANON ETONOGESTREL 1 Subdermal UNK 21529 IMPLANT
125926611 12592661 2 C PROTONIX PANTOPRAZOLE SODIUM 1 UNK 0
125926611 12592661 3 C WELLBUTRIN BUPROPION HYDROCHLORIDE 1 UNK 0
125926611 12592661 4 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125926611 12592661 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
125926611 12592661 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125926611 12592661 Acne
125926611 12592661 Complication associated with device
125926611 12592661 Incorrect drug administration duration
125926611 12592661 Menstruation irregular
125926611 12592661 Migration of implanted drug

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125926611 12592661 1 2013 0