The Safety Rates Drug Report

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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
125277261 12527726 1 I 20160524 20160628 20160705 20160705 EXP GXKR2016DE003022 SANDOZ 0.00 Y 0.00000 20160705 OT DE 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
125277261 12527726 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 10 MG, UNK Y 77040 10 MG
125277261 12527726 2 SS VANDETANIB. VANDETANIB 1 Oral 300 MG, UNK Y 0 300 MG
125277261 12527726 3 C BISOPROLOL HCT BISOPROLOL FUMARATEHYDROCHLOROTHIAZIDE 1 Oral 1 DF, UNK 0 1 DF
125277261 12527726 4 C LERCANIDIPINE LERCANIDIPINE 1 Oral 20 MG, UNK 0 20 MG
125277261 12527726 5 C EUTHYROX LEVOTHYROXINE SODIUM 1 Oral 0 100 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125277261 12527726 1 Depression
125277261 12527726 2 Product used for unknown indication
125277261 12527726 3 Hypertension
125277261 12527726 4 Hypertension
125277261 12527726 5 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
125277261 12527726 HO
125277261 12527726 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125277261 12527726 Acute kidney injury
125277261 12527726 Circulatory collapse
125277261 12527726 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
125277261 12527726 1 20160524 0