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
4263710 4061976 I 4263710-5 20031214 20031217 20040102 EXP EWC031237469 ELI LILLY AND COMPANY 25 YR F N 70 KG 20031224 MD

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
4263710 1004492605 PS XIGRIS 1 24 UG/KG/HR D
4263710 1004518780 C ZINACEF 1
4263710 1004518781 C ROCEPHIN 1
4263710 1004518782 C ZANTAC 1
4263710 1004518783 C CLEXANE (HEPARIN-FRACTION, SODIUM SALT) 2
4263710 1004518784 C CELESTON (BETAMETHASONE) 2
4263710 1004518785 C NORMOPRESAN (CLONIDINE HYDROCHLORIDE) 2
4263710 1004518786 C GARAMYCIN 1
4263710 1004518787 C DORMICUM (NITRAZEPAM) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4263710 1004492605 SEPSIS

Outcome of event

Event ID OUTC COD
4263710 OT

Reactions reported

Event ID PT
4263710 COMPLICATIONS OF MATERNAL EXPOSURE TO THERAPEUTIC DRUGS
4263710 PREMATURE RUPTURE OF MEMBRANES
4263710 UTERINE CONTRACTIONS DURING PREGNANCY

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

Event ID RPSR COD
4263710 FGN
4263710 HP
4263710 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4263710 1004492605 20031212 20031216