The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
126838941 12683894 1 I 20160806 20160817 20160825 20160825 EXP US-PFIZER INC-2016393545 PFIZER 75.00 YR F Y 63.50000 KG 20160825 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
126838941 12683894 1 PS CELEBREX CELECOXIB 1 UNK U 20998 CAPSULE, HARD
126838941 12683894 2 C DIAZEPAM. DIAZEPAM 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126838941 12683894 2 Sleep disorder

Outcome of event

Event ID CASEID OUTC COD
126838941 12683894 OT
126838941 12683894 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126838941 12683894 Anaphylactic reaction
126838941 12683894 Angioedema
126838941 12683894 Blood pressure decreased
126838941 12683894 Ear infection
126838941 12683894 Ear swelling
126838941 12683894 Erythema
126838941 12683894 Histamine level increased
126838941 12683894 Hypersensitivity
126838941 12683894 Lip swelling
126838941 12683894 Local swelling
126838941 12683894 Peripheral swelling
126838941 12683894 Pruritus
126838941 12683894 Swelling
126838941 12683894 Urticaria

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

no results found

Therapies reported

no results found