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
5120037 6148120 I 5120037-7 20051213 20060918 20060929 EXP 2006000029 PFIZER INC 59 YR M N 76 KG 20060928 MD GERMANY

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
5120037 1007726863 PS SUTENT 1 ORAL 37.5 MG (37.5 MG, 1 IN 1 D), ORAL Y D 21968
5120037 1007745894 C METOPROLOL (METOPROLOL) 2
5120037 1007745895 C LOCOL (FLUVASTATIN SODIUM) 2
5120037 1007745896 C ACETYLSALICYLIC ACID SRT 1
5120037 1007745897 C FOSAMAX 1
5120037 1007745898 C METOPROLOL TARTRATE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
5120037 1007726863 METASTATIC RENAL CELL CARCINOMA

Outcome of event

Event ID OUTC COD
5120037 HO
5120037 OT

Reactions reported

Event ID PT
5120037 DIZZINESS
5120037 FALL
5120037 VERTIGO
5120037 WOUND

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

Event ID RPSR COD
5120037 FGN
5120037 HP
5120037 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5120037 1007726863 20051213