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
119895982 11989598 2 F 201305 20151224 20160202 20160912 EXP CO-ASTELLAS-2015US045482 ASTELLAS 41.00 YR M Y 46.00000 KG 20160912 CN GB CO

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
119895982 11989598 1 PS AMPHOTERICIN B DEOXYCHOLATE AMPHOTERICIN B 1 Unknown UNK, UNKNOWN FREQ. 0 FORMULATION UNKNOWN
119895982 11989598 2 SS VIREAD TENOFOVIR DISOPROXIL FUMARATE 1 Unknown UNK, UNKNOWN FREQ. U 0 TABLET
119895982 11989598 3 C SULFAMETHOXAZOLE AND TRIMETHOPRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
119895982 11989598 4 C ITRACONAZOLE. ITRACONAZOLE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
119895982 11989598 5 C SPIRONOLACTONE. SPIRONOLACTONE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
119895982 11989598 6 C FTC EMTRICITABINE 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
119895982 11989598 7 C DARUNAVIR DARUNAVIR 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
119895982 11989598 8 C RITONAVIR. RITONAVIR 1 Unknown UNK UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN
119895982 11989598 9 C MfxHZE 2 Unknown UNK, UNKNOWN FREQ. U 0 FORMULATION UNKNOWN

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119895982 11989598 1 Histoplasmosis
119895982 11989598 2 HIV infection
119895982 11989598 3 Product used for unknown indication
119895982 11989598 4 Product used for unknown indication
119895982 11989598 5 Product used for unknown indication
119895982 11989598 6 Product used for unknown indication
119895982 11989598 7 Product used for unknown indication
119895982 11989598 8 Product used for unknown indication
119895982 11989598 9 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
119895982 11989598 DE
119895982 11989598 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119895982 11989598 Renal failure

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
119895982 11989598 2 201301 0