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
126188281 12618828 1 I 20120718 20140811 20160803 20160803 EXP JP-JNJFOC-20150311456 JANSSEN 35.36 YR A M Y 0.00000 20160803 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
126188281 12618828 1 SS PREZISTA DARUNAVIR ETHANOLATE 1 Oral N 0 400 MG TABLETS BID
126188281 12618828 2 PS PREZISTA DARUNAVIR ETHANOLATE 1 Oral N 21976 800 MG TABLETS QD
126188281 12618828 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 Oral 0 1 DF TABLET QD
126188281 12618828 4 SS NORVIR RITONAVIR 1 Oral 0 100 MG UNSPECIFIED QD
126188281 12618828 5 C CRAVIT LEVOFLOXACIN 1 Oral 0 1 DF TABLETS

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126188281 12618828 1 HIV infection
126188281 12618828 2 HIV infection
126188281 12618828 3 HIV infection
126188281 12618828 4 HIV infection
126188281 12618828 5 Infection prophylaxis

Outcome of event

Event ID CASEID OUTC COD
126188281 12618828 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126188281 12618828 Hyperkalaemia
126188281 12618828 Hyperphosphatasaemia
126188281 12618828 Hypertriglyceridaemia

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
126188281 12618828 1 20120704 0
126188281 12618828 2 20140128 0
126188281 12618828 3 20120704 0
126188281 12618828 4 20120704 0
126188281 12618828 5 20130401 0