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
127612411 12761241 1 I 20160912 20160920 20160920 EXP PL-ASTRAZENECA-2016SE97823 ASTRAZENECA 37.00 YR F Y 0.00000 20160920 MD PL PL

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
127612411 12761241 1 PS OMEPRAZOLE. OMEPRAZOLE 1 Oral U 19810
127612411 12761241 2 SS ROVAMYCINE SPIRAMYCIN 1 Unknown 9 MLN UNITS U 0
127612411 12761241 3 SS PIRIMETHAMINE PYRIMETHAMINE 1 Unknown 2 X 50 MG P.O U 0
127612411 12761241 4 SS SULPHADIAZINE SULFADIAZINE 1 Unknown 2 X 2000 MG U 0
127612411 12761241 5 SS FOLIC ACID. FOLIC ACID 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127612411 12761241 3 Toxoplasmosis
127612411 12761241 4 Toxoplasmosis

Outcome of event

Event ID CASEID OUTC COD
127612411 12761241 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127612411 12761241 Alanine aminotransferase increased
127612411 12761241 Aspartate aminotransferase increased
127612411 12761241 Exposure during pregnancy

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found