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
4503839 5676065 I 4503839-7 19980101 20041109 20041117 EXP US-MERCK-0411USA01749 MERCK HUMAN HEALTH DIVISION 56 YR F Y 20041118 MD

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
4503839 1005396252 PS VIOXX 1 ORAL
4503839 1005396253 SS VIOXX 1 ORAL
4503839 1005396254 SS VIOXX 1 ORAL
4503839 1005396255 C CALCIUM (UNSPECIFIED) 2 UNKNOWN
4503839 1005396256 C DIMETHYL SULFONE 2 UNKNOWN
4503839 1005396257 C CHONDROITIN 2 UNKNOWN
4503839 1005396258 C ESTROGENS (UNSPECIFIED) 2 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
4503839 1005396252 PAIN

Outcome of event

Event ID OUTC COD
4503839 OT

Reactions reported

Event ID PT
4503839 ARTHROPATHY
4503839 CEREBROVASCULAR ACCIDENT
4503839 OVERDOSE

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
4503839 1005396252 19980101 20040501
4503839 1005396253 19980101 20040501
4503839 1005396254 19980101 20040501
4503839 1005396258 20040801