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
126789121 12678912 1 I 20160803 20160805 20160824 20160824 EXP LK-ROCHE-1809950 ROCHE 3.00 YR M Y 14.00000 KG 20160824 MD LK LK

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
126789121 12678912 1 PS ROCEPHIN CEFTRIAXONE SODIUM 1 Intravenous (not otherwise specified) 63239 350 MG BID
126789121 12678912 2 SS ROCEPHIN CEFTRIAXONE SODIUM 1 63239
126789121 12678912 3 SS ROCEPHIN CEFTRIAXONE SODIUM 1 63239
126789121 12678912 4 C ATALINE 2 Oral 0 5 ML BID
126789121 12678912 5 C PIRITON CHLORPHENIRAMINE MALEATE 1 Oral 0 5 ML BID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126789121 12678912 1 White blood cell count increased
126789121 12678912 2 C-reactive protein increased
126789121 12678912 3 Lower respiratory tract infection

Outcome of event

Event ID CASEID OUTC COD
126789121 12678912 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
126789121 12678912 Blood pressure decreased
126789121 12678912 Cardiac arrest
126789121 12678912 Cardiac 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
126789121 12678912 1 20160803 20160803 0
126789121 12678912 4 20160802 0
126789121 12678912 5 20160802 0