The Safety Rates Drug Report

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Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5195429 6191677 F 5195429-0 20061212 20061214 20061230 EXP CA-NOVOPROD-259327 NOVOPROD 19 YR M Y 70 KG 20061230 OT 20061214 CANADA

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5195429 1007999351 PS NIASTASE 1 INTRAVENOUS 2.4 MG, SINGLE SU60160
5195429 1007999352 C VASOPRESSIN 2 INTRAVENOUS .24 U, QD
5195429 1007999353 C ADRENALINE /00003901/ 2 INTRAVENOUS 8.64 MG, QD
5195429 1007999354 C NOREPHEDRINE HYDROCHLORIDE 2 23.04 MG, QD
5195429 1007999355 C CIPROFLOXACIN 1 INTRAVENOUS 800 MG, QD
5195429 1007999356 C RANITIDINE 1 INTRAVENOUS 100 MG, QD
5195429 1007999357 C FLAGYL /00012501/ 2 INTRAVENOUS 1.5 G, QD

Indications of drugs used

Event ID DRUG SEQ INDI PT
5195429 1007999351 DISSEMINATED INTRAVASCULAR COAGULATION
5195429 1007999352 SHOCK HAEMORRHAGIC
5195429 1007999353 SHOCK HAEMORRHAGIC
5195429 1007999354 SHOCK HAEMORRHAGIC

Outcome of event

Event ID OUTC COD
5195429 DE
5195429 LT

Reactions reported

Event ID PT
5195429 DRUG INEFFECTIVE
5195429 SHOCK HAEMORRHAGIC

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5195429 1007999351 20061212
5195429 1007999352 20061212 20061212
5195429 1007999353 20061212 20061212
5195429 1007999354 20061212 20061212
5195429 1007999355 20061212 20061212
5195429 1007999357 20061212 20061212