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
127801811 12780181 1 I 20160904 0 20160926 20160926 DIR FDA-CTU 47.00 YR F N 62.65000 KG 20160925 N 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
127801811 12780181 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 30 TABLET(S) IN THE MORNING TAKEN BY MOUTH N D 0 30 DF COATED TABLET QD
127801811 12780181 3 C CIMZIA CERTOLIZUMAB PEGOL 1 0
127801811 12780181 4 C METOPROLOL. METOPROLOL 1 0
127801811 12780181 6 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 0
127801811 12780181 8 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 0
127801811 12780181 10 C CELEBREX CELECOXIB 1 0
127801811 12780181 12 C VIT B COMPLEX 2 0
127801811 12780181 14 C VITAMIN C ASCORBIC ACID 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127801811 12780181 1 Depression

Outcome of event

Event ID CASEID OUTC COD
127801811 12780181 DS
127801811 12780181 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127801811 12780181 Disturbance in attention
127801811 12780181 Dizziness
127801811 12780181 Impaired driving ability
127801811 12780181 Withdrawal syndrome

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

no results found

Therapies reported

no results found