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
125533101 12553310 1 I 20160415 20160705 20160713 20160713 EXP FR-JNJFOC-20160703774 JANSSEN 21.26 YR A M Y 50.00000 KG 20160713 OT FR FR

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
125533101 12553310 1 PS PREZISTA DARUNAVIR ETHANOLATE 1 Oral 1 IN THE MORNING AND 1 IN THE EVENING U U 21976 600 MG TABLETS BID
125533101 12553310 2 SS BACLOFENE BACLOFEN 1 Oral 1 IN THE MORNING 1 AT NOON AND 1 IN THE EVENING U 0 10 MG UNSPECIFIED TID
125533101 12553310 3 SS SUSTIVA EFAVIRENZ 1 Oral 1 IN THE EVENING U 0 600 MG COATED TABLET QD
125533101 12553310 4 SS NORVIR RITONAVIR 1 Unknown 1 IN THE MORNING AND 1 IN THE EVENING U 0 100 MG UNSPECIFIED BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125533101 12553310 1 HIV infection
125533101 12553310 2 HIV infection
125533101 12553310 3 HIV infection
125533101 12553310 4 HIV infection

Outcome of event

Event ID CASEID OUTC COD
125533101 12553310 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125533101 12553310 Hypoglycaemia
125533101 12553310 Hypothermia

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found