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
108801493 10880149 3 F 2009 20160706 20150302 20160712 EXP FR-009507513-1402FRA012315 MERCK 0.00 F Y 70.00000 KG 20160712 CN FR FR

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
108801493 10880149 1 PS IMPLANON ETONOGESTREL 1 Subcutaneous 1 DF, UNKNOWN, LEFT ARM Y 21529 1 DF IMPLANT
108801493 10880149 2 SS IMPLANON ETONOGESTREL 1 Subdermal 1 DF, UNKNOWN Y 21529 1 DF IMPLANT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108801493 10880149 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
108801493 10880149 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108801493 10880149 Amenorrhoea
108801493 10880149 Complication associated with device
108801493 10880149 Device difficult to use
108801493 10880149 Device embolisation
108801493 10880149 Difficulty removing drug implant
108801493 10880149 Incorrect drug administration duration
108801493 10880149 Medical device removal
108801493 10880149 Migration of implanted drug
108801493 10880149 Progesterone increased
108801493 10880149 Weight increased

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
108801493 10880149 1 200906 201511 0
108801493 10880149 2 2009 0