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
125484961 12548496 1 I 20160524 20160629 20160712 20160712 EXP DE-BFARM-16217168 DE-WATSON-2016-14429 WATSON 74.00 YR F Y 57.20000 KG 20160712 CN 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
125484961 12548496 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 10 MG, UNKNOWN Y UNCONFIRMED 77034 10 MG UNK
125484961 12548496 2 SS VANDETANIB. VANDETANIB 1 Oral 300 MG, UNKNOWN Y 0 300 MG
125484961 12548496 3 C BISOPROLOL HCT BISOPROLOL FUMARATEHYDROCHLOROTHIAZIDE 1 Oral 1 DF, UNKNOWN U 0 1 DF
125484961 12548496 4 C LERCANIDIPINE LERCANIDIPINE 1 Oral 20 MG, UNKNOWN U 0 20 MG
125484961 12548496 5 C EUTHYROX LEVOTHYROXINE SODIUM 1 Oral 100 ?G, UNKNOWN U 0 100 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125484961 12548496 1 Depression
125484961 12548496 2 Product used for unknown indication
125484961 12548496 3 Hypertension
125484961 12548496 4 Hypertension
125484961 12548496 5 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
125484961 12548496 HO
125484961 12548496 LT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125484961 12548496 Acute kidney injury
125484961 12548496 Circulatory collapse
125484961 12548496 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
125484961 12548496 1 20160524 0