The Safety Rates Drug Report

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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
124636952 12463695 2 F 2016 20160620 20160614 20160705 PER US-PFIZER INC-2016282926 PFIZER 27.00 YR F Y 61.00000 KG 20160705 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
124636952 12463695 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 1 DF, 1X/DAY 21992 1 DF PROLONGED-RELEASE TABLET QD
124636952 12463695 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, 1X/DAY (AT BED) 21992 50 MG PROLONGED-RELEASE TABLET QD
124636952 12463695 3 SS CYMBALTA DULOXETINE HYDROCHLORIDE 1 UNK 0
124636952 12463695 4 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 100 UG, 1X/DAY 0 100 UG QD
124636952 12463695 5 C LORYNA DROSPIRENONEETHINYL ESTRADIOL 1 1 DF, 1X/DAY 0 1 DF TABLET QD
124636952 12463695 6 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 10 MG, 1X/DAY 0 10 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124636952 12463695 1 Depression
124636952 12463695 2 Anxiety
124636952 12463695 4 Thyroid disorder
124636952 12463695 5 Contraception
124636952 12463695 6 Seasonal allergy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124636952 12463695 Abdominal distension
124636952 12463695 Diarrhoea
124636952 12463695 Drug withdrawal syndrome
124636952 12463695 Pain
124636952 12463695 Reaction to drug excipients

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
124636952 12463695 1 201510 0