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
125702852 12570285 2 F 2015 20160729 20160719 20160803 EXP FR-PFIZER INC-2016341147 PFIZER 58.00 YR F Y 0.00000 20160803 OT FR FR

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
125702852 12570285 1 PS Effexor LP VENLAFAXINE HYDROCHLORIDE 1 Oral 75 MG, DAILY Y 20699 75 MG PROLONGED-RELEASE CAPSULE
125702852 12570285 2 SS XANAX ALPRAZOLAM 1 Oral ONE TABLET IN THE MORNING, HALF A TABLET AT NOON AND ONE TABLET IN THE EVENING Y 18276 TABLET TID
125702852 12570285 3 SS IMOVANE ZOPICLONE 1 Oral 7.5 MG, DAILY Y 0 7.5 MG
125702852 12570285 4 SS VALDOXAN AGOMELATINE 1 Oral 25 MG, 1X/DAY Y 0 25 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125702852 12570285 1 Depression
125702852 12570285 2 Depression
125702852 12570285 3 Depression
125702852 12570285 4 Depression

Outcome of event

Event ID CASEID OUTC COD
125702852 12570285 DS
125702852 12570285 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125702852 12570285 Acute respiratory failure
125702852 12570285 Chronic respiratory failure
125702852 12570285 Cyanosis
125702852 12570285 Dyspnoea
125702852 12570285 Interstitial lung disease
125702852 12570285 Oxygen saturation decreased
125702852 12570285 Pulmonary hypertension

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
125702852 12570285 1 201307 201505 0
125702852 12570285 2 201505 0
125702852 12570285 3 201505 0
125702852 12570285 4 2010 201505 0