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
127401151 12740115 1 I 20150731 20160909 20160913 20160913 EXP US-ABBVIE-16P-163-1725610-00 ABBVIE 36.00 YR F Y 0.00000 20160913 OT COUNTRY NOT SPECIFIED US

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
127401151 12740115 1 PS KALETRA LOPINAVIRRITONAVIR 1 Oral 1 COURSE EARLIEST EXPOSURE FIRST TRIMESTER UNKNOWN 21226 1 DF SOFT CAPSULE QID
127401151 12740115 2 SS COMBIVIR LAMIVUDINEIDOVUDINE 1 Oral 1 COURSE EARLIEST EXPOSURE FIRST TRIMESTER UNKNOWN 0 1 DF BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127401151 12740115 1 HIV infection
127401151 12740115 2 HIV infection

Outcome of event

Event ID CASEID OUTC COD
127401151 12740115 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127401151 12740115 Abortion spontaneous
127401151 12740115 Exposure during pregnancy
127401151 12740115 Foetal death

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
127401151 12740115 1 20150610 0
127401151 12740115 2 20160610 0