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
125468541 12546854 1 I 20160621 20160705 20160711 20160711 EXP FR-ELI_LILLY_AND_COMPANY-FR201607001163 ELI LILLY AND CO 77.20 YR M Y 0.00000 20160708 CN FR FR

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
125468541 12546854 1 PS PROZAC FLUOXETINE HYDROCHLORIDE 1 Oral 20 MG, EACH EVENING U U 18936 20 MG DISPERSIBLE TABLET QD
125468541 12546854 2 SS TAMSULOSINE TAMSULOSIN HYDROCHLORIDE 1 Oral 0.4 DF, EACH EVENING U 0 .4 DF QD
125468541 12546854 3 SS BISOPROLOL BISOPROLOL 1 Oral 5 MG, QD U 0 5 MG QD
125468541 12546854 4 C PREVISCAN /00261401/ PENTOXIFYLLINE 1 Oral 75 DF, EACH EVENING N 0 75 DF TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125468541 12546854 1 Depression
125468541 12546854 2 Benign prostatic hyperplasia
125468541 12546854 3 Hypertension
125468541 12546854 4 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
125468541 12546854 OT
125468541 12546854 LT
125468541 12546854 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125468541 12546854 Clumsiness
125468541 12546854 Cognitive disorder
125468541 12546854 Coma
125468541 12546854 Disturbance in attention
125468541 12546854 Fall
125468541 12546854 Subdural haematoma

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found