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
127562681 12756268 1 I 20140801 20160905 20160916 20160916 EXP ZA-GILEAD-2016-0233074 GILEAD 0.00 M Y 41.00000 KG 20160916 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
127562681 12756268 1 PS EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, QD 21937 1 DF TABLET QD
127562681 12756268 2 SS POTASSIUM POTASSIUM 1 Oral 600 MG, QD 0 600 MG QD
127562681 12756268 3 SS SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Oral 960 MG, QD 0 960 MG QD
127562681 12756268 4 SS VITAMINS /00067501/ VITAMINS 1 Oral 1 DF, QD 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127562681 12756268 1 HIV infection
127562681 12756268 2 Hypokalaemia
127562681 12756268 3 Prophylaxis
127562681 12756268 4 Malnutrition

Outcome of event

Event ID CASEID OUTC COD
127562681 12756268 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127562681 12756268 Gastroenteritis

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
127562681 12756268 1 20140731 0
127562681 12756268 2 20140731 0
127562681 12756268 3 20140729 0
127562681 12756268 4 20140731 0