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
125851131 12585113 1 I 20160709 20160719 20160723 20160723 EXP GB-MHRA-ADR 23561391 GB-ACCORD-042674 ACCORD 39.00 YR F Y 80.00000 KG 20160723 MD 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
125851131 12585113 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 U 202553
125851131 12585113 2 C ADALAT NIFEDIPINE 1 Oral 224.96 DF 0 1 DF QD
125851131 12585113 3 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 Oral EACH MORNING. 2 DF 0 1 DF QD
125851131 12585113 4 C LOSARTAN. LOSARTAN 1 Oral 256.96 DF 0 1 DF QD
125851131 12585113 5 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) 0 2 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125851131 12585113 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125851131 12585113 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125851131 12585113 Eye pain
125851131 12585113 Headache
125851131 12585113 Photophobia

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
125851131 12585113 1 20160520 0
125851131 12585113 2 20151127 20160520 0
125851131 12585113 3 20160711 0
125851131 12585113 4 20151026 0
125851131 12585113 5 20151026 0