The Safety Rates Drug Report

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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
126820032 12682003 2 F 20160722 20160830 20160824 20160908 EXP ZA-ABBVIE-16P-143-1702774-00 ABBVIE 34.00 YR F Y 69.80000 KG 20160908 MD COUNTRY NOT SPECIFIED ZA

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
126820032 12682003 1 PS RITONAVIR. RITONAVIR 1 Oral 20945 100 MG SOFT CAPSULE QD
126820032 12682003 2 C ATAZANAVIR ATAZANAVIR 1 Oral 0 300 MG QD
126820032 12682003 3 C EMTRICITABINE W/TENOFOVIR EMTRICITABINETENOFOVIR DISOPROXIL 1 Oral 0 QD
126820032 12682003 4 C FOLIC ACID. FOLIC ACID 1 0
126820032 12682003 5 C MULTIVITAMIN VITAMINS 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126820032 12682003 1 HIV infection
126820032 12682003 2 HIV infection
126820032 12682003 3 HIV infection
126820032 12682003 4 Product used for unknown indication
126820032 12682003 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126820032 12682003 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126820032 12682003 Caesarean section
126820032 12682003 Exposure during pregnancy
126820032 12682003 Gestational hypertension

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
126820032 12682003 1 20160406 0
126820032 12682003 2 20160406 0
126820032 12682003 3 20160406 0