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
125379381 12537938 1 I 20150911 20160624 20160707 20160707 EXP DE-TEVA-672064GER TEVA 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
125379381 12537938 1 PS CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Transplacental DOSAGE UNKNOWN 77232
125379381 12537938 2 SS TWYNSTA AMLODIPINE BESYLATETELMISARTAN 1 Transplacental 1 DOSAGE FORMS DAILY; 1 DOSAGE FORM CONTAINS 5 MG AMLODIPINE AND 40 MG TELMISARTAN 0 1 DF QD
125379381 12537938 3 SS METHYLDOPA. METHYLDOPA 1 Transplacental 750 MILLIGRAM DAILY; 0 250 MG TID
125379381 12537938 4 C Folio FOLIC ACID 1 Transplacental .4 MILLIGRAM DAILY; 0 .4 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125379381 12537938 1 Depression
125379381 12537938 2 Hypertension
125379381 12537938 3 Hypertension
125379381 12537938 4 Prophylaxis of neural tube defect

Outcome of event

Event ID CASEID OUTC COD
125379381 12537938 CA
125379381 12537938 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125379381 12537938 Foetal exposure during pregnancy
125379381 12537938 Foot deformity
125379381 12537938 Hypospadias
125379381 12537938 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
125379381 12537938 1 20141210 20150911 0
125379381 12537938 2 20141210 20150212 0
125379381 12537938 3 20150213 20150911 0
125379381 12537938 4 20141210 20150911 0