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
77934262 7793426 2 F 20110105 20130917 20110131 20130930 EXP NL-MEDIMMUNE-MEDI-0012353 MEDIMMUNE 7.00 MON M Y 0.00000 20130930 CN US NL

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
77934262 7793426 1 PS SYNAGIS 1 INTRAMUSCULAR D 103770 15 MG/KG INJECTION /month
77934262 7793426 2 SS SYNAGIS 1 INTRAMUSCULAR D 103770 15 MG/KG INJECTION /month

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
77934262 7793426 1 Antiviral prophylaxis
77934262 7793426 2 Antiviral prophylaxis

Outcome of event

Event ID CASEID OUTC COD
77934262 7793426 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
77934262 7793426 Diarrhoea
77934262 7793426 Dyspnoea
77934262 7793426 Respiratory tract infection

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
77934262 7793426 1 20101001 20101222 0
77934262 7793426 2 20110121 0