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
98551994 9855199 4 F 20110422 20160816 20140130 20160826 PER US-BAYER-2014-013379 BAYER 36.00 YR A F Y 160.54000 KG 20160826 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
98551994 9855199 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
98551994 9855199 2 C PROZAC FLUOXETINE HYDROCHLORIDE 1 0
98551994 9855199 3 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 0
98551994 9855199 4 C CELEXA CITALOPRAM HYDROBROMIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98551994 9855199 1 Contraception
98551994 9855199 3 Hypertension
98551994 9855199 4 Depression

Outcome of event

Event ID CASEID OUTC COD
98551994 9855199 LT
98551994 9855199 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
98551994 9855199 Abdominal pain lower
98551994 9855199 Anhedonia
98551994 9855199 Anxiety
98551994 9855199 Depression
98551994 9855199 Emotional distress
98551994 9855199 General physical health deterioration
98551994 9855199 Injury
98551994 9855199 Pain
98551994 9855199 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
98551994 9855199 1 20100422 20110422 0