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
125639631 12563963 1 I 20160704 20160713 20160717 20160717 EXP GB-DEXPHARM-20161513 DEXCEL 20.00 YR A F Y 66.00000 KG 20160717 OT GB GB

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
125639631 12563963 1 PS OMEPRAZOLE. OMEPRAZOLE 1 U U 0
125639631 12563963 2 C DESOGESTREL DESOGESTREL 1 DAILY DOSE: 1 DF DOSAGE FORM EVERY DAYS 21 DF 0 1 DF QD
125639631 12563963 3 C DIHYDROCODEINE DIHYDROCODEINE 1 THREE TIMES DAILY. 0 5 ML
125639631 12563963 4 SS LANSOPRAZOLE. LANSOPRAZOLE 1 DAILY DOSE: 0.5 DF DOSAGE FORM EVERY DAYS 2.5 DF U U 0 .5 DF QD
125639631 12563963 5 C Microgynon ETHINYL ESTRADIOLLEVONORGESTREL ACETATE 1 DAILY DOSE: 1 DF DOSAGE FORM EVERY DAYS 164.958333 DF 0 1 DF QD
125639631 12563963 6 SS RANITIDINE. RANITIDINE 1 DAILY DOSE: 2 DF DOSAGE FORM EVERY DAYS 124 DF U U 0 1 DF BID
125639631 12563963 7 C SUMATRIPTAN. SUMATRIPTAN 1 AS DIRECTED. 0 1 DF

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
125639631 12563963 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125639631 12563963 Dizziness

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
125639631 12563963 1 20160428 0
125639631 12563963 2 20160613 0
125639631 12563963 3 20160609 20160610 0
125639631 12563963 4 20160629 0
125639631 12563963 5 20160121 20160629 0
125639631 12563963 6 20160503 0
125639631 12563963 7 20160613 20160616 0