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
6809369 7405827 F 6809369-1 20100330 20100621 20100630 EXP SE-ASTRAZENECA-2010SE23514 AZPRODUW00 20757 DY F Y 99 KG 20100630 MD 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
6809369 1014003094 PS OMEPRAZOLE 1 ORAL 19810
6809369 1014003095 SS CELEBRA 2 ORAL
6809369 1014003096 SS INVESTIGATIONAL DRUG 2 ORAL
6809369 1014003097 SS INVESTIGATIONAL DRUG 2 ORAL
6809369 1014003098 C DOXYCYCLINE 1
6809369 1014003099 C LEVOTHYROXINE SODIUM 1
6809369 1014003100 C SYMBICORT 1
6809369 1014003101 C VISCOTEARS 2
6809369 1014003102 C METHOTREXATE 1
6809369 1014003103 C FOLACIN 2
6809369 1014003104 C ATACAND 1
6809369 1014003105 C FELODIPINE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6809369 1014003094 PROPHYLAXIS AGAINST GASTROINTESTINAL ULCER
6809369 1014003095 RHEUMATOID ARTHRITIS
6809369 1014003096 RHEUMATOID ARTHRITIS
6809369 1014003098 RESPIRATORY TRACT INFECTION

Outcome of event

Event ID OUTC COD
6809369 HO

Reactions reported

Event ID PT
6809369 AMNESIA
6809369 HYPONATRAEMIA
6809369 HYPOPHOSPHATAEMIA
6809369 RESPIRATORY TRACT INFECTION

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
6809369 1014003094 20060101
6809369 1014003095 20070101
6809369 1014003096 20091214 20100401 109 DAY
6809369 1014003097 20100415
6809369 1014003098 20100322 20100330 9 DAY
6809369 1014003099 20031010
6809369 1014003100 20060101
6809369 1014003101 20061010
6809369 1014003102 20060823
6809369 1014003103 20060823