The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
5587769 6465179 I 5587769-8 20070927 20070928 20071231 EXP AEUSA200700224 TALECRIS BIOTHERAPEUTICS, INC. 54 YR F N 115 LBS 20071228 UNITED STATES

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
5587769 1009383508 PS PROLASTIN 1 INTRAVENOUS 1110 MG;QW;IV D D 26N8WT1 20100523
5587769 1009398867 C LEXAPRO 1
5587769 1009398868 C LAMIVUDINE 1
5587769 1009398869 C PROGRAF 1
5587769 1009398870 C MYFORTIC 1
5587769 1009398871 C PREDNISONE TAB 1
5587769 1009398872 C VALTREX 1
5587769 1009398873 C ZITHROMAX 1
5587769 1009398874 C MEPRON 1
5587769 1009398875 C IMMUNE GLOBULIN INTRAVENOUS (HUMAN) 1
5587769 1009398876 C PRILOSEC 1
5587769 1009398877 C PRENATAL VITAMINS 2
5587769 1009398878 C VIACTIV 2
5587769 1009398879 C MYCELEX 1
5587769 1009398880 C OXYCODONE 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
5587769 1009383508 ALPHA-1 ANTI-TRYPSIN DEFICIENCY

Outcome of event

Event ID OUTC COD
5587769 HO
5587769 OT

Reactions reported

Event ID PT
5587769 EAR PAIN
5587769 ERYTHEMA
5587769 HYPOAESTHESIA ORAL
5587769 MUSCLE SPASMS
5587769 PARAESTHESIA ORAL
5587769 SINUSITIS BACTERIAL
5587769 STAPHYLOCOCCAL INFECTION

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

Event ID RPSR COD
5587769 CSM
5587769 HP
5587769 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5587769 1009383508 20070901 20071004