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
127181071 12718107 1 I 20120523 20130802 20160906 20160906 EXP JP-009507513-1308JPN003929 MERCK 67.00 YR M Y 0.00000 20160906 MD JP JP

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
127181071 12718107 1 PS ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral 800 MG, QD, DIVIDED DOSE FREQUENCY UNKNOWN 22145 800 MG TABLET QD
127181071 12718107 2 SS ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral 800 MG, QD, DIVIDED DOSE FREQUENCY UNKNOWN 22145 800 MG TABLET QD
127181071 12718107 3 SS EPZICOM ABACAVIR SULFATELAMIVUDINE 1 Oral 1 (DOSAGE FORM), QD, DIVIDED DOSE FREQUENCY UNKNOWN 0 1 DF TABLET QD
127181071 12718107 4 C JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 50 MG, QD U 0 50 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127181071 12718107 1 HIV infection
127181071 12718107 3 HIV infection
127181071 12718107 4 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
127181071 12718107 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127181071 12718107 Atrial fibrillation
127181071 12718107 Hyperlipidaemia
127181071 12718107 Lower limb fracture

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
127181071 12718107 1 20090217 20090624 0
127181071 12718107 2 20091112 20140614 0
127181071 12718107 3 20090625 20150414 0