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
127050311 12705031 1 I 20160828 0 20160831 20160831 DIR 39.00 YR F N 152.00000 LBS 20160829 N 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
127050311 12705031 1 PS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 Oral N Y 0 30 DF COATED TABLET QD
127050311 12705031 2 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 0
127050311 12705031 4 C ALTENOLOL 2 0
127050311 12705031 6 C PROZAC FLUOXETINE HYDROCHLORIDE 1 0
127050311 12705031 8 C SEROQUEL QUETIAPINE FUMARATE 1 0
127050311 12705031 10 C TOPAMAX TOPIRAMATE 1 0
127050311 12705031 12 C GABAPENTIN. GABAPENTIN 1 0
127050311 12705031 14 C NORITHEDRONE 2 0
127050311 12705031 16 C MAGNESIUM MAGNESIUM 1 0
127050311 12705031 18 C RIBOFLAVIN RIBOFLAVIN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127050311 12705031 1 Major depression

Outcome of event

Event ID CASEID OUTC COD
127050311 12705031 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127050311 12705031 Migraine with aura
127050311 12705031 Nausea
127050311 12705031 Withdrawal syndrome

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

no results found

Therapies reported

no results found