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
98552494 9855249 4 F 20160817 20140130 20160823 PER US-BAYER-2014-014153 BAYER 36.00 YR A F Y 58.50000 KG 20160823 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
98552494 9855249 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
98552494 9855249 2 SS MIRENA LEVONORGESTREL 1 UNK 21225 INTRAUTERINE DELIVERY SYSTEM
98552494 9855249 3 C AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 0
98552494 9855249 4 C DARVOCET-N 100 ACETAMINOPHENPROPOXYPHENE NAPSYLATE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
98552494 9855249 1 Contraception
98552494 9855249 2 Contraception

Outcome of event

Event ID CASEID OUTC COD
98552494 9855249 LT
98552494 9855249 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
98552494 9855249 Abdominal pain lower
98552494 9855249 Anhedonia
98552494 9855249 Device use issue
98552494 9855249 General physical health deterioration
98552494 9855249 Injury
98552494 9855249 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
98552494 9855249 1 20050729 20120229 0
98552494 9855249 3 20080819 0
98552494 9855249 4 20080819 0