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
127028551 12702855 1 I 20130503 20160804 20160831 20160831 EXP ZA-VIIV HEALTHCARE LIMITED-ZA2016122522 VIIV 31.00 YR F Y 0.00000 20160831 MD ZA 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
127028551 12702855 1 SS ATRIPLA EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNK 0 TABLET
127028551 12702855 2 SS TENOFOVIR DISOPROXIL FUMARATE. TENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNK Y 0 TABLET
127028551 12702855 3 SS Efavirenz EFAVIRENZ 1 Unknown UNK Y 0
127028551 12702855 4 PS LAMIVUDINE. LAMIVUDINE 1 Unknown UNK Y 20564
127028551 12702855 5 SS ALUVIA LOPINAVIRRITONAVIR 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127028551 12702855 1 HIV infection
127028551 12702855 2 HIV infection
127028551 12702855 3 HIV infection
127028551 12702855 4 HIV infection
127028551 12702855 5 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127028551 12702855 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127028551 12702855 Caesarean section
127028551 12702855 Exposure during pregnancy
127028551 12702855 Normal newborn

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
127028551 12702855 2 20110317 20130826 0
127028551 12702855 3 20110317 20130826 0
127028551 12702855 4 20110317 20130826 0
127028551 12702855 5 20130826 0