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
125240821 12524082 1 I 20150407 20160624 20160704 20160704 EXP JP-009507513-1606JPN013558 MERCK 78.00 YR M Y 0.00000 20160704 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
125240821 12524082 1 PS ISENTRESS RALTEGRAVIR POTASSIUM 1 Oral 800 MG DAILY, DIVIDED DOSE FREQUENCY UNKNOWN 22145 800 MG TABLET QD
125240821 12524082 2 SS EPZICOM ABACAVIR SULFATELAMIVUDINE 1 1 TABLET, QD 0 1 DF TABLET QD
125240821 12524082 3 C OLOPATADINE HYDROCHLORIDE. OLOPATADINE HYDROCHLORIDE 1 Oral 5 MG, BID U 0 5 MG TABLET BID
125240821 12524082 4 C AMLODIPINE AMLODIPINE BESYLATE 1 Oral 5 MG, QD U 0 5 MG TABLET QD
125240821 12524082 5 C ENALAPRIL MALEATE. ENALAPRIL MALEATE 1 Oral 5 MG, QD U 0 5 MG TABLET QD
125240821 12524082 6 C FUROSEMIDE. FUROSEMIDE 1 Oral 20 MG, QD U 0 20 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125240821 12524082 1 HIV infection
125240821 12524082 2 HIV infection
125240821 12524082 3 Seborrhoeic dermatitis
125240821 12524082 4 Hypertension
125240821 12524082 5 Hypertension
125240821 12524082 6 Renal disorder

Outcome of event

Event ID CASEID OUTC COD
125240821 12524082 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125240821 12524082 Dyslipidaemia
125240821 12524082 Weight 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
125240821 12524082 1 20130611 0
125240821 12524082 2 20130611 0
125240821 12524082 6 20151218 0