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
125488192 12548819 2 F 20160525 20160802 20160712 20160808 EXP FR-AFSSAPS-CN20160423 FR-GLAXOSMITHKLINE-FR2016GSK094341 GLAXOSMITHKLINE 77.62 YR M Y 0.00000 20160808 OT FR FR

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
125488192 12548819 1 PS Zelitrex VALACYCLOVIR HYDROCHLORIDE 1 Oral UNK Y 20487
125488192 12548819 2 SS Zelitrex VALACYCLOVIR HYDROCHLORIDE 1 Oral UNK Y 20487
125488192 12548819 3 SS ALLOPURINOL. ALLOPURINOL 1 Oral 200 MG, QD Y 0 200 MG QD
125488192 12548819 4 SS PRIMPERAN METOCLOPRAMIDE HYDROCHLORIDE 1 Oral 10 MG, PRN Y 0 10 MG
125488192 12548819 5 SS Flecaine FLECAINIDE 1 Oral 150 MG, 1D 0 150 MG QD
125488192 12548819 6 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) UNK Y 0 375 MG/M**2
125488192 12548819 7 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) SECOND COURSE OF RITUXIMAB (1 INJECTION OF 500 MG/M2 MONTHLY Y 0 500 MG/M**2
125488192 12548819 8 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) THIRD COURSE OF RITUXIMAB (1 INJECTION OF 500 MG/M2 MONTHLY Y 0 500 MG/M**2
125488192 12548819 9 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) 1 INJECTION OF 500 MG/M2 MONTHLY Y 0 500 MG/M**2
125488192 12548819 10 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) FIFTH COURSE OF RITUXIMAB Y 0 500 MG/M**2
125488192 12548819 11 SS MABTHERA RITUXIMAB 1 Intravenous (not otherwise specified) 500 MG/M2, UNK Y 0 500 MG/M**2
125488192 12548819 12 SS XARELTO RIVAROXABAN 1 Oral 15 MG, UNK Y 0 15 MG
125488192 12548819 13 SS ZYDELIG IDELALISIB 1 Oral 150 MG, Z Y 0 150 MG
125488192 12548819 14 SS ZYDELIG IDELALISIB 1 Oral 150 MG, BID Y 0 150 MG BID
125488192 12548819 15 SS ZYDELIG IDELALISIB 1 Oral 150 MG, BID Y 0 150 MG BID
125488192 12548819 16 SS ZYDELIG IDELALISIB 1 Oral 150 MG, BID Y 0 150 MG BID
125488192 12548819 17 SS ZYDELIG IDELALISIB 1 Oral 150 MG, BID Y 0 150 MG BID
125488192 12548819 18 C BISOPROLOL BISOPROLOL 1 U 0
125488192 12548819 19 C Lercanidipine LERCANIDIPINE 1 0
125488192 12548819 20 C Atorvastatin ATORVASTATIN 1 UNK 0
125488192 12548819 21 C BACTRIM SULFAMETHOXAZOLETRIMETHOPRIM 1 1 UNK, Z 0 1 DF

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125488192 12548819 1 Prophylaxis
125488192 12548819 3 Product used for unknown indication
125488192 12548819 4 Nausea
125488192 12548819 5 Transient ischaemic attack
125488192 12548819 6 Lymphoma
125488192 12548819 12 Transient ischaemic attack
125488192 12548819 13 Lymphoma

Outcome of event

Event ID CASEID OUTC COD
125488192 12548819 HO
125488192 12548819 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125488192 12548819 Dermatitis exfoliative

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
125488192 12548819 1 201601 20160525 0
125488192 12548819 2 201601 20160525 0
125488192 12548819 3 201601 20160525 0
125488192 12548819 4 201601 20160525 0
125488192 12548819 5 20160104 0
125488192 12548819 6 20160104 20160525 0
125488192 12548819 7 20160201 0
125488192 12548819 8 20160301 0
125488192 12548819 9 20160330 0
125488192 12548819 10 20160427 0
125488192 12548819 11 20160525 0
125488192 12548819 12 20160104 2016 0
125488192 12548819 13 20160104 20160525 0
125488192 12548819 14 20160301 0
125488192 12548819 15 20160330 0
125488192 12548819 16 20160427 0
125488192 12548819 17 20160525 0
125488192 12548819 20 20160525 0
125488192 12548819 21 201601 20160120 0