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
125929601 12592960 1 I 201510 20151105 20160726 20160726 PER US-ABBVIE-15P-163-1496237-00 ABBVIE 92.45 YR F Y 0.00000 20160726 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
125929601 12592960 1 PS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral Y UNKNOWN,UNKNOWN 21402 88 UG TABLET QD
125929601 12592960 2 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402 75 UG TABLET QD
125929601 12592960 3 SS SYNTHROID LEVOTHYROXINE SODIUM 1 Oral UNKNOWN 21402 75 UG QD
125929601 12592960 4 C METOPROLOL. METOPROLOL 1 0
125929601 12592960 5 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125929601 12592960 1 Hypothyroidism
125929601 12592960 2 Hypothyroidism
125929601 12592960 4 Product used for unknown indication
125929601 12592960 5 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125929601 12592960 Blood thyroid stimulating hormone increased
125929601 12592960 Fatigue
125929601 12592960 Hypoaesthesia
125929601 12592960 Hypoaesthesia oral
125929601 12592960 Product quality issue

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
125929601 12592960 1 20151022 20151023 0
125929601 12592960 2 1938 20151021 0