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
5117573 6139096 F 5117573-6 20060904 20060905 20060929 EXP JP-ROCHE-463283 ROCHE 56 YR M Y 20060929 MD JAPAN

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
5117573 1007716900 PS ROCALTROL 1 INTRAVENOUS 018044
5117573 1007716901 SS ROCALTROL 1 INTRAVENOUS 018044
5117573 1007716902 C RENAGEL 1 ORAL
5117573 1007716903 C PANALDINE 2 ORAL
5117573 1007716904 C SOLANAX 2 ORAL
5117573 1007716905 C LENDORMIN 2 ORAL
5117573 1007716906 C ALLOZYM 2 ORAL
5117573 1007716907 C DORNER 2 ORAL
5117573 1007716908 C PARIET 2 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5117573 1007716900 HYPERPARATHYROIDISM SECONDARY

Outcome of event

Event ID OUTC COD
5117573 OT

Reactions reported

Event ID PT
5117573 GAMMA-GLUTAMYLTRANSFERASE INCREASED
5117573 HEPATIC FUNCTION ABNORMAL

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
5117573 1007716900 20060707 20060809 34 DAY
5117573 1007716901 20060811 20060904 25 DAY
5117573 1007716902 20031024
5117573 1007716903 20031024
5117573 1007716904 20031024
5117573 1007716905 20031024
5117573 1007716906 20031024
5117573 1007716907 20031128
5117573 1007716908 20040810