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
108615366 10861536 6 F 20120620 20160816 20150223 20160822 EXP JP-JNJFOC-20150212299 JANSSEN 32.00 YR A M Y 0.00000 20160822 MD JP JP

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
108615366 10861536 1 PS PREZISTA DARUNAVIR ETHANOLATE 1 Oral N 21976 400 MG TABLETS BID
108615366 10861536 2 SS NORVIR RITONAVIR 1 Oral 0 100 MG UNSPECIFIED QD
108615366 10861536 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 0 1 DF TABLET QD
108615366 10861536 4 C VALTREX VALACYCLOVIR HYDROCHLORIDE 1 Oral 0 1000 MG TABLET BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108615366 10861536 1 HIV infection
108615366 10861536 2 HIV infection
108615366 10861536 3 HIV infection
108615366 10861536 4 Genital herpes

Outcome of event

Event ID CASEID OUTC COD
108615366 10861536 HO
108615366 10861536 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108615366 10861536 Chest discomfort
108615366 10861536 Face oedema
108615366 10861536 Genital herpes
108615366 10861536 Headache
108615366 10861536 Nausea
108615366 10861536 Syphilis

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
108615366 10861536 1 20120620 0
108615366 10861536 2 20120620 0
108615366 10861536 3 20120620 0
108615366 10861536 4 20131113 20131118 0