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
127762491 12776249 1 I 20160902 20160919 20160923 20160923 EXP US-ABBVIE-16P-163-1732671-00 ABBVIE 0.00 DY M Y 0.00000 20160923 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
127762491 12776249 1 PS RITONAVIR. RITONAVIR 1 Transplacental D UNKNOWN 20945
127762491 12776249 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Transplacental D UNKNOWN 0
127762491 12776249 3 SS PREZISTA DARUNAVIR ETHANOLATE 1 Transplacental D UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127762491 12776249 1 Maternal exposure timing unspecified
127762491 12776249 2 Maternal exposure timing unspecified
127762491 12776249 3 Maternal exposure timing unspecified

Outcome of event

Event ID CASEID OUTC COD
127762491 12776249 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
127762491 12776249 Cerebral haemorrhage
127762491 12776249 Failure to thrive
127762491 12776249 Foetal exposure during pregnancy
127762491 12776249 Low birth weight baby
127762491 12776249 Premature baby

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

no results found

Therapies reported

no results found