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
125390081 12539008 1 I 20160524 20160628 20160708 20160708 EXP DE-DRREDDYS-GER/GER/16/0081097 DR REDDYS 74.00 YR F Y 57.20000 KG 20160708 MD 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
125390081 12539008 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral Y U UNKNOWN 77038 10 MG
125390081 12539008 2 SS VANDETANIB. VANDETANIB 1 Oral Y U 0 300 MG
125390081 12539008 3 C Bisoprolol/HCT 2 Oral 0 1 DF
125390081 12539008 4 C Lercanidipin LERCANIDIPINE 1 Oral 0 20 MG
125390081 12539008 5 C Euthyrox LEVOTHYROXINE SODIUM 1 Oral 0 100 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125390081 12539008 1 Depression
125390081 12539008 2 Product used for unknown indication
125390081 12539008 3 Hypertension
125390081 12539008 4 Hypertension
125390081 12539008 5 Hypothyroidism

Outcome of event

Event ID CASEID OUTC COD
125390081 12539008 LT
125390081 12539008 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125390081 12539008 Acute kidney injury
125390081 12539008 Circulatory collapse
125390081 12539008 Decreased appetite
125390081 12539008 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
125390081 12539008 1 20160524 0