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
125582551 12558255 1 I 20160415 20160707 20160714 20160714 EXP FR-ABBVIE-16P-056-1674189-00 ABBVIE 21.26 YR M Y 50.00000 KG 20160714 MD 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
125582551 12558255 1 PS NORVIR RITONAVIR 1 Oral U UNKNOWN 22417 100 MG TABLET BID
125582551 12558255 2 SS SUSTIVA EFAVIRENZ 1 Oral U UNKNOWN 0 600 MG TABLET QD
125582551 12558255 3 SS PREZISTA DARUNAVIR ETHANOLATE 1 Oral U UNKNOWN 0 600 MG TABLET BID
125582551 12558255 4 SS BACLOFENE BACLOFEN 1 Oral U UNKNOWN 0 10 MG TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125582551 12558255 1 Product used for unknown indication
125582551 12558255 2 Product used for unknown indication
125582551 12558255 3 Product used for unknown indication
125582551 12558255 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125582551 12558255 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125582551 12558255 Hypoglycaemia
125582551 12558255 Hypothermia

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

no results found

Therapies reported

no results found