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
123564903 12356490 3 F 20160509 20160722 20160511 20160726 PER US-BAYER-2016-090675 BAYER 24.00 YR A F Y 0.00000 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
123564903 12356490 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT TU017EV 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
123564903 12356490 2 SS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT TU0183H 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
123564903 12356490 3 C IBUPROFEN. IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123564903 12356490 1 Contraception
123564903 12356490 2 Contraception
123564903 12356490 3 Abdominal pain lower

Outcome of event

Event ID CASEID OUTC COD
123564903 12356490 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123564903 12356490 Complication of device insertion
123564903 12356490 Post procedural haemorrhage
123564903 12356490 Procedural pain
123564903 12356490 Vaginal haemorrhage

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
123564903 12356490 1 20160509 20160509 0
123564903 12356490 2 20160601 0