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
121007323 12100732 3 F 20160730 20160222 20160810 PER US-009507513-1602USA009856 MERCK 29.00 YR F Y 0.00000 20160810 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
121007323 12100732 1 PS ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral UNK 22145 TABLET
121007323 12100732 2 SS ISENTRESS RALTEGRAVIR POTASSIUM 1 22145 TABLET
121007323 12100732 3 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 UNK 0
121007323 12100732 4 SS TRUVADA EMTRICITABINETENOFOVIR DISOPROXIL FUMARATE 1 0
121007323 12100732 5 SS HARVONI LEDIPASVIRSOFOSBUVIR 1 UNK 0
121007323 12100732 6 SS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 UNK 0
121007323 12100732 7 C ANCEF CEFAZOLIN SODIUM 1 UNK U 0
121007323 12100732 8 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 UNK U 0
121007323 12100732 9 C COLACE DOCUSATE SODIUM 1 UNK U 0
121007323 12100732 10 C SIMETHICONE (DIMETHICONE) DIMETHICONE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121007323 12100732 1 HIV infection
121007323 12100732 2 Hepatitis C
121007323 12100732 3 HIV infection
121007323 12100732 4 Hepatitis C

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121007323 12100732 Exposure during pregnancy

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
121007323 12100732 1 20121201 0
121007323 12100732 3 20121201 0