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
6733439 7394054 I 6733439-X 20091219 20100512 20100520 EXP FR-KINGPHARMUSA00001-K201000588 KINGPHARMUSA00001 82 YR F Y 20100520 CN FRANCE

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
6733439 1013719545 PS ALTACE 1 ORAL 1.25 MG, UNK 19901
6733439 1013719546 SS OFLOCET 2 ORAL UNK
6733439 1013719547 SS RIFADIN 1 ORAL UNK
6733439 1013719548 SS ESOMEPRAZOLE 2 ORAL UNK
6733439 1013719549 SS TRIFLUCAN 2 ORAL UNK
6733439 1013719550 C VASTAREL 2 UNK
6733439 1013719551 C LEVOTHYROXINE SODIUM 1
6733439 1013719552 C FENOFIBRATE 2 UNK
6733439 1013719553 C ASPEGIC 1000 1 UNK
6733439 1013719554 C CALCIPARINE 1 UNK
6733439 1013719555 C ZOLPIDEM 1 UNK
6733439 1013719556 C SPASFON 2 UNK
6733439 1013719557 C DAFALGAN 2 UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
6733439 1013719546 ARTHRITIS BACTERIAL
6733439 1013719547 ARTHRITIS BACTERIAL

Outcome of event

Event ID OUTC COD
6733439 HO

Reactions reported

Event ID PT
6733439 ANAEMIA
6733439 INFLAMMATION
6733439 LEUKOPENIA
6733439 NEUTROPENIA

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
6733439 1013719545 20091210 20100317 98 DAY
6733439 1013719546 20091120 20100312 113 DAY
6733439 1013719547 20091120 20100312 113 DAY
6733439 1013719548 20091120 20100311 112 DAY
6733439 1013719549 20091211 20100311 91 DAY
6733439 1013719550 20091120 20100311 112 DAY
6733439 1013719552 20091120 20100311 112 DAY
6733439 1013719553 20091120
6733439 1013719554 20091201
6733439 1013719555 20091201
6733439 1013719556 20091201
6733439 1013719557 20091201