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
7023069 7547153 F 7023069-7 20100701 20100921 20100930 EXP US-PFIZER INC-2010101341 PFIZERINC 77 YR F Y 59 KG 20100930 PH 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
7023069 1014812595 PS CAMPTOSAR 1 UNK 20571
7023069 1014812596 SS FLUOROURACIL 2 UNK
7023069 1014812597 SS OXALIPLATIN 2 UNK
7023069 1014812598 SS GEMZAR 1 UNK
7023069 1014812599 SS LEUCOVORIN CALCIUM 1 UNK
7023069 1014812600 C SYNTHROID 1 ORAL 100 MCG OR 175 MCG
7023069 1014812601 C ZOFRAN 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7023069 1014812595 PANCREATIC CARCINOMA METASTATIC
7023069 1014812596 PANCREATIC CARCINOMA METASTATIC
7023069 1014812597 PANCREATIC CARCINOMA METASTATIC
7023069 1014812598 PANCREATIC CARCINOMA METASTATIC
7023069 1014812599 PANCREATIC CARCINOMA METASTATIC
7023069 1014812600 HYPOTHYROIDISM

Outcome of event

Event ID OUTC COD
7023069 OT

Reactions reported

Event ID PT
7023069 AUTOIMMUNE THROMBOCYTOPENIA
7023069 CONTUSION
7023069 PETECHIAE
7023069 PLATELET COUNT DECREASED

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
7023069 1014812595 20090101 20100801
7023069 1014812596 20090101 20100804
7023069 1014812597 20090101 20100101
7023069 1014812598 20090101 20100804
7023069 1014812599 20090101 20100804