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
125448881 12544888 1 I 20160524 20160628 20160711 20160711 EXP DE-BFARM-16217168 DE-FRI-1000085959 FOREST 74.00 YR F Y 57.20000 KG 20160711 OT DK DE

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
125448881 12544888 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral Y 20822 10 MG
125448881 12544888 2 SS VANDETANIB / VANDETANIB VANDETANIB 1 Oral Y 0 300 MG
125448881 12544888 3 C Bisoprolol/HCT 5 mg / 12.5 mg / Bisoprol fumarate, hydroclorothiazide 2 Oral 0 1 DF
125448881 12544888 4 C LERCANIDIPIN LERCANIDIPINE 1 Oral 0 20 MG
125448881 12544888 5 C Euthyrox / Levothyroxine sodium 2 Oral 0 100 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125448881 12544888 1 Depression
125448881 12544888 2 Product used for unknown indication
125448881 12544888 3 Hypertension
125448881 12544888 4 Hypertension
125448881 12544888 5 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
125448881 12544888 HO
125448881 12544888 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125448881 12544888 Acute kidney injury
125448881 12544888 Circulatory collapse
125448881 12544888 Electrocardiogram QT prolonged

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
125448881 12544888 1 20160524 2016 0