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
125375431 12537543 1 I 20151028 20160707 20160707 PER US-AMAG PHARMACEUTICALS, INC.-AMAG201501198 AMAG 0.00 Y 0.00000 20160707 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
125375431 12537543 1 PS FERAHEME FERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE 1 Intravenous drip UNK UNK 22180 INJECTION
125375431 12537543 2 C Fluoxetine hcl FLUOXETINE HYDROCHLORIDE 1 Oral 40 MG, UNK 0 40 MG
125375431 12537543 3 SS CELEBREX CELECOXIB 1 Oral 200 MG, UNK 0 200 MG
125375431 12537543 4 C OMEPRAZOLE. OMEPRAZOLE 1 Oral 40 MG, UNK 0 40 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125375431 12537543 1 Product used for unknown indication
125375431 12537543 2 Depression
125375431 12537543 3 Inflammation

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125375431 12537543 Hypoaesthesia
125375431 12537543 Iron overload
125375431 12537543 Pain in extremity

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
125375431 12537543 1 201007 0
125375431 12537543 2 1998 0