The Safety Rates Drug Report

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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
126899202 12689920 2 F 20160829 20160826 20160831 EXP JP-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-55540NB BOEHRINGER INGELHEIM 83.00 YR M Y 0.00000 20160831 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
126899202 12689920 1 PS MICARDIS TELMISARTAN 1 Unknown 20 MG 20850 20 MG TABLET QD
126899202 12689920 2 SS PNEUMOVAX 23 PNEUMOCOCCAL VACCINE, POLYVALENT 23 1 Intravenous (not otherwise specified) 0.5 ML U 0 .5 ML INJECTION QD
126899202 12689920 3 SS SODIUM RABEPRAZOLE RABEPRAZOLE SODIUM 1 Oral U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126899202 12689920 1 Product used for unknown indication
126899202 12689920 2 Product used for unknown indication
126899202 12689920 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126899202 12689920 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126899202 12689920 Interstitial lung disease
126899202 12689920 Sepsis

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
126899202 12689920 1 201501 201505 0