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
126055351 12605535 1 I 20160709 20160719 20160729 20160729 EXP GB-MHRA-TPP5362204C423755YC1468233368505 GB-TEVA-679604ACC TEVA 39.00 YR F Y 80.00000 KG 20160729 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
126055351 12605535 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 U U 76846
126055351 12605535 2 C ADALAT NIFEDIPINE 1 Oral 1 DOSAGE FORMS DAILY; 224.958333 DF 0 1 DF QD
126055351 12605535 3 C BENDROFLUMETHIAZIDE BENDROFLUMETHIAZIDE 1 Oral 1 DOSAGE FORMS DAILY; EACH MORNING. 2 DF 0 1 DF QD
126055351 12605535 4 C LOSARTAN. LOSARTAN 1 Oral 1 DOSAGE FORMS DAILY; 256.958333 DF 0 1 DF QD
126055351 12605535 5 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) 0 2 DF

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126055351 12605535 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126055351 12605535 Eye pain
126055351 12605535 Headache
126055351 12605535 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
126055351 12605535 1 20160520 0
126055351 12605535 2 20151127 20160520 0
126055351 12605535 3 20160711 0
126055351 12605535 4 20151026 0
126055351 12605535 5 20151026 0