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
125404485 12540448 5 F 20160819 20160708 20160824 PER US-PFIZER INC-2016334875 PFIZER 53.00 YR F Y 68.00000 KG 20160824 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
125404485 12540448 1 SS ENBREL ETANERCEPT 1 SHOT, IN HER THIGH Y 0
125404485 12540448 2 PS SULFASALAZINE. SULFASALAZINE 1 UNK Y 7073
125404485 12540448 3 C PREMPRO ESTROGENS, CONJUGATEDMEDROXYPROGESTERONE ACETATE 1 Oral UNK, 1X/DAY 0 TABLET QD
125404485 12540448 4 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 20 MG, 1X/DAY 0 20 MG CAPSULE QD
125404485 12540448 5 C DICLOFENAC DICLOFENAC 1 Oral 75 MG, 1X/DAY 0 75 MG TABLET QD
125404485 12540448 6 C CITALOPRAM CITALOPRAM HYDROBROMIDE 1 Oral 20 MG, 1X/DAY 0 20 MG TABLET QD
125404485 12540448 7 C SUMATRIPTAN. SUMATRIPTAN 1 Oral 100 MG, AS NEEDED 0 100 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125404485 12540448 3 Hormone therapy
125404485 12540448 4 Gastrooesophageal reflux disease
125404485 12540448 5 Rheumatoid arthritis
125404485 12540448 6 Depression
125404485 12540448 7 Migraine

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125404485 12540448 Drug hypersensitivity
125404485 12540448 Pain
125404485 12540448 Pruritus
125404485 12540448 Swelling
125404485 12540448 Urticaria

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
125404485 12540448 1 201606 0