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
127773761 12777376 1 I 201508 20160915 20160924 20160924 PER US-009507513-1609USA008752 MERCK 46.00 YR M Y 0.00000 20160924 CN US 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
127773761 12777376 1 PS ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral UNK U 22145 TABLET
127773761 12777376 2 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127773761 12777376 1 HIV infection

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127773761 12777376 CD4 lymphocytes decreased
127773761 12777376 CD4 lymphocytes increased
127773761 12777376 Lymphocyte count increased

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
127773761 12777376 1 201401 0