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
123568843 12356884 3 F 201604 20160722 20160511 20160728 EXP US-PFIZER INC-2016238248 PFIZER 54.00 YR F Y 0.00000 20160728 MD 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
123568843 12356884 1 PS NEURONTIN GABAPENTIN 1 300 MG, 1X/DAY Y 20235 300 MG QD
123568843 12356884 2 SS MELOXICAM. MELOXICAM 1 15 MG, 2X/DAY Y 0 15 MG TABLET BID
123568843 12356884 3 C SYNTHROID LEVOTHYROXINE SODIUM 1 112 UG, DAILY 0 112 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123568843 12356884 1 Trigeminal neuralgia

Outcome of event

Event ID CASEID OUTC COD
123568843 12356884 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123568843 12356884 Bone pain
123568843 12356884 Local swelling
123568843 12356884 Lymphadenopathy
123568843 12356884 Oral disorder
123568843 12356884 Oropharyngeal pain
123568843 12356884 Product use issue
123568843 12356884 Swelling face
123568843 12356884 Swollen tongue

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
123568843 12356884 1 201604 20160603 0
123568843 12356884 2 201604 20160426 0