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
125947091 12594709 1 I 20160709 20160719 20160726 20160726 EXP GB-MHRA-TPP5362204C423755YC1468233368505 GB-DRREDDYS-GER/UKI/16/0081667 DR REDDYS 39.00 YR F Y 80.00000 KG 20160726 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
125947091 12594709 1 PS AMLODIPINE AMLODIPINE BESYLATE 1 U U UNKNOWN 76692
125947091 12594709 2 C ADALAT NIFEDIPINE 1 Oral 224.958333 DF 0 1 DF QD
125947091 12594709 3 C Bendroflumethiazide BENDROFLUMETHIAZIDE 1 Oral 2 DF 0 1 DF QD
125947091 12594709 4 C LOSARTAN. LOSARTAN 1 Oral 256.958333 DF 0 1 DF QD
125947091 12594709 5 C VENTOLIN ALBUTEROL SULFATE 1 Respiratory (inhalation) 0 2 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125947091 12594709 1 Product used for unknown indication
125947091 12594709 2 Product used for unknown indication
125947091 12594709 3 Product used for unknown indication
125947091 12594709 4 Product used for unknown indication
125947091 12594709 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125947091 12594709 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125947091 12594709 Eye pain
125947091 12594709 Headache
125947091 12594709 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
125947091 12594709 1 20160520 0
125947091 12594709 2 20151127 20160520 0
125947091 12594709 3 20160711 0
125947091 12594709 4 20151026 0
125947091 12594709 5 20151026 0