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
125573561 12557356 1 I 20160518 20160705 20160714 20160714 EXP GB-MHRA-ADR 23540912 GB-MYLANLABS-2016M1028136 MYLAN 0.00 Y 0.00000 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
125573561 12557356 1 PS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK U 202650 5 MG
125573561 12557356 2 C FULTIUM D3 2 Oral 800 IU, UNK U 0 800 IU
125573561 12557356 3 C TAMSULOSIN TAMSULOSIN 1 Oral 400 ?G, UNK U 0 400 UG
125573561 12557356 4 C FINASTERIDE. FINASTERIDE 1 Oral 5 MG, UNK U 0 5 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125573561 12557356 1 Osteoporosis
125573561 12557356 2 Osteoporosis
125573561 12557356 3 Prostatic disorder
125573561 12557356 4 Prostatic disorder

Outcome of event

Event ID CASEID OUTC COD
125573561 12557356 DS
125573561 12557356 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125573561 12557356 Eye pain
125573561 12557356 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
125573561 12557356 1 20160516 20160516 0