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
122565764 12256576 4 F 20160305 20160730 20160412 20160808 EXP US-009507513-1604USA002032 MERCK 0.00 DY F Y 2.35000 KG 20160808 CN US US

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
122565764 12256576 1 PS ISENTRESS RALTEGRAVIR POTASSIUM 1 Transplacental UNK 22145 TABLET
122565764 12256576 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
122565764 12256576 OT
122565764 12256576 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
122565764 12256576 Cleft palate
122565764 12256576 Cytogenetic abnormality
122565764 12256576 Foetal exposure during pregnancy
122565764 12256576 Heart disease congenital
122565764 12256576 Low birth weight baby
122565764 12256576 Talipes

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

no results found

Therapies reported

no results found