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
126188701 12618870 1 I 20160330 20160729 20160803 20160803 EXP FR-ROCHE-1805502 ROCHE 80.00 YR M Y 0.00000 20160803 MD 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
126188701 12618870 1 PS Rocephine CEFTRIAXONE SODIUM 1 Intravenous (not otherwise specified) Y 63239
126188701 12618870 2 SS TAVANIC LEVOFLOXACIN 1 Oral Y 0
126188701 12618870 3 SS MICARDIS PLUS HYDROCHLOROTHIAZIDETELMISARTAN 1 Oral U 0
126188701 12618870 4 C PREVISCAN (FRANCE) FLUINDIONE 1 Oral 0 15 MG QD
126188701 12618870 5 C TRIFLUCAN FLUCONAZOLE 1 Oral 0 400 MG QD
126188701 12618870 6 C EUPANTOL PANTOPRAZOLE SODIUM 1 Oral 0 20 MG QD
126188701 12618870 7 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126188701 12618870 1 Lung disorder
126188701 12618870 2 Lung disorder
126188701 12618870 3 Product used for unknown indication
126188701 12618870 4 Atrial fibrillation

Outcome of event

Event ID CASEID OUTC COD
126188701 12618870 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126188701 12618870 Acute kidney injury

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
126188701 12618870 1 20160329 20160330 0
126188701 12618870 2 20160328 20160407 0
126188701 12618870 3 20160329 0
126188701 12618870 4 20160330 0
126188701 12618870 5 20160319 20160328 0