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
112548696 11254869 6 F 20160701 20150709 20160707 EXP US-ABBVIE-15P-163-1419506-00 ABBVIE 0.00 M Y 0.00000 20160707 OT COUNTRY NOT SPECIFIED 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
112548696 11254869 1 PS NORVIR RITONAVIR 1 Transplacental UNKNOWN 22417
112548696 11254869 2 SS ATRIPLA EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNKNOWN 0
112548696 11254869 3 SS REYATAZ ATAZANAVIR SULFATE 1 Transplacental UNKNOWN 0
112548696 11254869 4 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental UNKNOWN 0
112548696 11254869 5 SS STRIBILD COBICISTATELVITEGRAVIREMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
112548696 11254869 1 Maternal exposure timing unspecified
112548696 11254869 2 Maternal exposure timing unspecified
112548696 11254869 3 Maternal exposure timing unspecified
112548696 11254869 4 Maternal exposure timing unspecified
112548696 11254869 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
112548696 11254869 DE
112548696 11254869 CA
112548696 11254869 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
112548696 11254869 Abortion induced
112548696 11254869 Congenital bladder anomaly
112548696 11254869 Foetal 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