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
125353471 12535347 1 I 20150911 20160624 20160707 20160707 EXP DE-DRREDDYS-GER/GER/16/0081034 DR REDDYS 1.00 DY M Y 3.15000 KG 20160707 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
125353471 12535347 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Transplacental UNKNOWN 77038
125353471 12535347 2 SS TWYNSTA AMLODIPINE BESYLATETELMISARTAN 1 Transplacental 0 40 MG QD
125353471 12535347 3 SS METHYLDOPA. METHYLDOPA 1 Transplacental 0 250 MG TID
125353471 12535347 4 C Folio FOLIC ACID 1 Transplacental 0 .4 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125353471 12535347 1 Depression
125353471 12535347 2 Hypertension
125353471 12535347 3 Hypertension
125353471 12535347 4 Prophylaxis of neural tube defect

Outcome of event

Event ID CASEID OUTC COD
125353471 12535347 CA
125353471 12535347 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125353471 12535347 Foetal exposure during pregnancy
125353471 12535347 Foot deformity
125353471 12535347 Hypospadias
125353471 12535347 Kinematic imbalances due to suboccipital strain

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
125353471 12535347 1 20141210 20150911 0
125353471 12535347 2 20141210 20150212 0
125353471 12535347 3 20150213 20150911 0
125353471 12535347 4 20141210 20150911 0