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
97840654 9784065 4 F 201108 20160830 20131226 20160907 EXP US-BAYER-2013-156443 BAYER 43.00 YR A F Y 60.00000 KG 20160907 OT 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
97840654 9784065 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT 447558 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
97840654 9784065 2 C FLOVENT FLUTICASONE PROPIONATE 1 UNK 0
97840654 9784065 3 C DIPHENOXYLATE/ATROPINE [DIPHENOXYLATE HYDROCHLORIDE] 2 0
97840654 9784065 4 C PROAIR HFA ALBUTEROL SULFATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97840654 9784065 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
97840654 9784065 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
97840654 9784065 Abdominal pain upper
97840654 9784065 Device issue
97840654 9784065 Device use issue
97840654 9784065 Diarrhoea haemorrhagic
97840654 9784065 Gastrointestinal injury
97840654 9784065 Injury
97840654 9784065 Pain

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
97840654 9784065 1 20050826 20110921 0
97840654 9784065 2 1999 2013 0