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
125552031 12555203 1 I 20160518 20160705 20160714 20160714 EXP GB-MHRA-ADR 23540912 GB-DRREDDYS-GER/UKI/16/0081240 DR REDDYS 85.00 YR M Y 70.00000 KG 20160714 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
125552031 12555203 1 PS Zoledronic acid ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) U UNKNOWN 91363 5 MG INFUSION
125552031 12555203 2 C FULTIUM-D3 2 Oral 0 800 IU
125552031 12555203 3 C TAMSULOSIN TAMSULOSIN 1 Oral 0 400 UG
125552031 12555203 4 C FINASTERIDE. FINASTERIDE 1 Oral 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125552031 12555203 1 Osteoporosis
125552031 12555203 2 Osteoporosis
125552031 12555203 3 Prostatic disorder
125552031 12555203 4 Prostatic disorder

Outcome of event

Event ID CASEID OUTC COD
125552031 12555203 OT
125552031 12555203 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
125552031 12555203 Eye pain
125552031 12555203 Headache

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
125552031 12555203 1 20160516 20160516 0