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
5943912 7033072 I 5943912-X 20081021 20081104 PER 2008S1019094 MYLAN PHARMACEUTICALS INC. 74 YR M N 20081030 OT 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
5943912 1010670547 PS FUROSEMIDE INTENSOL 1 40735
5943912 1010707609 SS HYDROCHLOROTHIAZIDE 1
5943912 1010707610 SS LENALIDOMIDE 2 ORAL 5 MG; DAILY; ORAL
5943912 1010707611 SS LENALIDOMIDE 2 ORAL 10 MG; DAILY; ORAL
5943912 1010707612 C EPOGEN 1 40735
5943912 1010707613 C WARFARIN 2 40735
5943912 1010707614 SS HYDROXYCARBAMIDE 2 40735
5943912 1010707616 C ASCORBIC ACID 1 40735
5943912 1010707621 C FOLIC ACID 1 40735
5943912 1010707625 C CYANOCOBALAMIN 1 40735
5943912 1010707627 C FERROUS FUMARATE 1 40735
5943912 1010707631 C TRINSICON 2 40735
5943912 1010707633 C LEVOTHYROXINE SODIUM 1 40735

Indications of drugs used

Event ID DRUG SEQ INDI PT
5943912 1010670547 MYELODYSPLASTIC SYNDROME
5943912 1010707609 MYELODYSPLASTIC SYNDROME
5943912 1010707610 MYELODYSPLASTIC SYNDROME
5943912 1010707611 MYELODYSPLASTIC SYNDROME

Outcome of event

Event ID OUTC COD
5943912 OT

Reactions reported

Event ID PT
5943912 BLOOD CREATININE INCREASED
5943912 BLOOD UREA INCREASED
5943912 FATIGUE
5943912 NEPHROLITHIASIS
5943912 RENAL IMPAIRMENT

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

Event ID RPSR COD
5943912 CSM
5943912 HP
5943912 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
5943912 1010707610 20080530
5943912 1010707611 20060530 20060801
5943912 1010707611 20080225 20080430