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
106561236 10656123 6 F 2005 20160927 20141216 20160929 PER US-BAYER-2014-183241 BAYER 27.00 YR A F Y 157.37000 KG 20160929 LW 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
106561236 10656123 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT 42375 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
106561236 10656123 2 C ADIPEX-P PHENTERMINE HYDROCHLORIDE 1 UNK 0
106561236 10656123 3 C PROZAC FLUOXETINE HYDROCHLORIDE 1 UNK 0
106561236 10656123 4 C VICODIN ACETAMINOPHENHYDROCODONE BITARTRATE 1 0
106561236 10656123 5 C IBUPROFEN. IBUPROFEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
106561236 10656123 1 Contraception
106561236 10656123 2 Weight decreased

Outcome of event

Event ID CASEID OUTC COD
106561236 10656123 HO
106561236 10656123 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
106561236 10656123 Abdominal pain lower
106561236 10656123 Back pain
106561236 10656123 Complication of device removal
106561236 10656123 Device breakage
106561236 10656123 Device issue
106561236 10656123 Genital haemorrhage
106561236 10656123 Infertility female
106561236 10656123 Injury
106561236 10656123 Pelvic inflammatory disease
106561236 10656123 Uterine perforation

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
106561236 10656123 1 20050228 20070305 0
106561236 10656123 2 20070227 0
106561236 10656123 3 20070227 0