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
125415533 12541553 3 F 20160705 20160818 20160708 20160823 EXP US-PFIZER INC-2016336119 PFIZER 46.00 YR F Y 57.15000 KG 20160823 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
125415533 12541553 1 PS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 125 MG, (INJECTION IN THE BOTTOM; 2 DOSES) Y 11856 125 MG POWDER FOR SOLUTION FOR INFUSION
125415533 12541553 2 SS SOLU-MEDROL METHYLPREDNISOLONE SODIUM SUCCINATE 1 Y 11856 POWDER FOR SOLUTION FOR INFUSION
125415533 12541553 3 C BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE 1 25MG TABLET; EVERY FOUR TO SIX HOURS 476484 0 25 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125415533 12541553 1 Food allergy
125415533 12541553 2 Hypersensitivity
125415533 12541553 3 Rash

Outcome of event

Event ID CASEID OUTC COD
125415533 12541553 HO
125415533 12541553 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125415533 12541553 Dysphemia
125415533 12541553 Dyspnoea
125415533 12541553 Fatigue
125415533 12541553 Gait disturbance
125415533 12541553 Heart rate increased
125415533 12541553 Hypoaesthesia
125415533 12541553 Insomnia
125415533 12541553 Muscle spasms
125415533 12541553 Palpitations
125415533 12541553 Paraesthesia
125415533 12541553 Seizure

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
125415533 12541553 1 20160705 0
125415533 12541553 3 20160629 20160715 0