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
116331344 11633134 4 F 20150217 20160905 20151015 20160909 EXP ZA-GILEAD-2015-0176579 GILEAD 66.00 YR E M Y 60.00000 KG 20160909 OT 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
116331344 11633134 1 PS EFAVIRENZ/EMTRICITABINE/TENOFOVIR DISOPROXIL FUMARATE EFAVIRENZEMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 1 DF, QD 6 DF 21937 1 DF TABLET QD
116331344 11633134 2 SS FUROSEMIDE. FUROSEMIDE 1 Oral 40 MG, UNK 0 40 MG BID
116331344 11633134 3 SS FUROSEMIDE. FUROSEMIDE 1 0
116331344 11633134 4 C POTASSIUM /00031402/ POTASSIUM 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
116331344 11633134 1 HIV infection
116331344 11633134 2 Cardiac failure congestive
116331344 11633134 3 Diuretic therapy
116331344 11633134 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
116331344 11633134 DE
116331344 11633134 HO
116331344 11633134 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
116331344 11633134 Acute kidney injury
116331344 11633134 Cardiac failure congestive
116331344 11633134 Hypernatraemia
116331344 11633134 Renal impairment

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
116331344 11633134 1 20150211 20150302 0
116331344 11633134 2 20150217 20150224 0