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
6394242 7126590 F 1 6394242-6 20080617 20090929 20091006 EXP WAES 0909USA00484 MERCK + CO., INC. 86 YR F N 20091005 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
6394242 1012400199 PS FOSAMAX 1 ORAL 35 MG WKY PO U D 20560
6394242 1012455573 SS PEON (ZALTOPROFEN) 2 ORAL 80 MG TID PO U U
6394242 1012455580 SS MECOBALAMIN 2 ORAL 1500 MICROGM TID PO U U
6394242 1012455582 SS OPALMON (LIMAPROST) 2 ORAL 5 MICROGM TID PO U U
6394242 1012455583 SS ALFAROL (ALFACALCIDOL) 2 ORAL 1 MICROGRAM DAILY PO U U

Indications of drugs used

Event ID DRUG SEQ INDI PT
6394242 1012400199 OSTEOPOROSIS
6394242 1012455573 LUMBAR SPINAL STENOSIS
6394242 1012455580 LUMBAR SPINAL STENOSIS
6394242 1012455582 LUMBAR SPINAL STENOSIS
6394242 1012455583 OSTEOPOROSIS

Outcome of event

Event ID OUTC COD
6394242 OT

Reactions reported

Event ID PT
6394242 RENAL IMPAIRMENT

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

Event ID RPSR COD
6394242 FGN
6394242 HP
6394242 OTH
6394242 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6394242 1012400199 20070308 20080617 468 DAY
6394242 1012455573 20070306 20080603 456 DAY
6394242 1012455580 20070306 20080603 456 DAY
6394242 1012455582 20070306 20080603 456 DAY
6394242 1012455583 20070306 20080603 456 DAY