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
125323482 12532348 2 F 201606 20160727 20160706 20160803 EXP US-ABBVIE-16P-163-1668741-00 ABBVIE 98.91 YR M Y 0.00000 20160803 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
125323482 12532348 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN 21402 TABLET
125323482 12532348 2 C NIFEDIPINE. NIFEDIPINE 1 Unknown UNKNOWN 0
125323482 12532348 3 C FLOMAX TAMSULOSIN HYDROCHLORIDE 1 Unknown UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125323482 12532348 1 Hypothyroidism
125323482 12532348 2 Hypertension
125323482 12532348 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125323482 12532348 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125323482 12532348 Agitation
125323482 12532348 Arthralgia
125323482 12532348 Back pain
125323482 12532348 Blood pressure increased
125323482 12532348 Blood thyroid stimulating hormone decreased
125323482 12532348 Depression
125323482 12532348 Drug dose omission
125323482 12532348 Dry skin
125323482 12532348 Eye swelling
125323482 12532348 Overdose
125323482 12532348 Skin exfoliation
125323482 12532348 Transient ischaemic attack

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
125323482 12532348 1 201603 0