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
97022214 9702221 4 F 20130315 20160901 20131121 20160906 PER US-BAYER-2013-141029 BAYER 34.00 YR A F Y 98.87000 KG 20160906 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
97022214 9702221 1 PS MIRENA LEVONORGESTREL 1 Intra-uterine 20 MCG/24HR, CONT TU008K5 21225 20 UG INTRAUTERINE DELIVERY SYSTEM
97022214 9702221 2 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 150 MCG 0
97022214 9702221 3 C MICARDIS TELMISARTAN 1 Oral 90 MG, UNK 0 90 MG
97022214 9702221 4 C METOPROLOL. METOPROLOL 1 Oral 25 MG, UNK 0 25 MG
97022214 9702221 5 C EDARBYCLOR AZILSARTAN KAMEDOXOMILCHLORTHALIDONE 1 Oral 80 MG, UNK 0 80 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
97022214 9702221 1 Contraception

Outcome of event

Event ID CASEID OUTC COD
97022214 9702221 OT
97022214 9702221 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
97022214 9702221 Abdominal pain
97022214 9702221 Device issue
97022214 9702221 Genital haemorrhage
97022214 9702221 Injury
97022214 9702221 Pain
97022214 9702221 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
97022214 9702221 1 20110403 20130315 0