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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125929541 | 12592954 | 1 | I | 2010 | 20151119 | 20160726 | 20160726 | PER | US-ABBVIE-15P-163-1505500-00 | ABBVIE | 0.00 | F | Y | 68.00000 | KG | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125929541 | 12592954 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Unknown | UNKNOWN | 21402 | 75 | UG | QD | |||||||
125929541 | 12592954 | 2 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Unknown | UNKNOWN | 21402 | QD | |||||||||
125929541 | 12592954 | 3 | SS | LIOTHYRONINE SODIUM. | LIOTHYRONINE SODIUM | 1 | Oral | UNKNOWN | 0 | 2.5 | UG | QD | |||||||
125929541 | 12592954 | 4 | SS | LIOTHYRONINE SODIUM. | LIOTHYRONINE SODIUM | 1 | Oral | UNKNOWN | 0 | 2.5 | UG | QD | |||||||
125929541 | 12592954 | 5 | SS | LEVOTHYROXINE SODIUM. | LEVOTHYROXINE SODIUM | 1 | Unknown | U | UNKNOWN | 0 | 75 | UG | QD | ||||||
125929541 | 12592954 | 6 | C | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | Unknown | 0 | 40 | MG | |||||||||
125929541 | 12592954 | 7 | C | RANITIDINE. | RANITIDINE | 1 | Unknown | 0 | 150 | MG | |||||||||
125929541 | 12592954 | 8 | C | PRAVASTATIN. | PRAVASTATIN | 1 | Unknown | 0 | |||||||||||
125929541 | 12592954 | 9 | C | NITROGLYCERINE | NITROGLYCERIN | 1 | Transdermal | 0 | |||||||||||
125929541 | 12592954 | 10 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | 0 | 5 | MG | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125929541 | 12592954 | 1 | Product used for unknown indication |
125929541 | 12592954 | 2 | Hypothyroidism |
125929541 | 12592954 | 3 | Hypothyroidism |
125929541 | 12592954 | 5 | Product used for unknown indication |
125929541 | 12592954 | 6 | Product used for unknown indication |
125929541 | 12592954 | 7 | Product used for unknown indication |
125929541 | 12592954 | 8 | Product used for unknown indication |
125929541 | 12592954 | 9 | Product used for unknown indication |
125929541 | 12592954 | 10 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125929541 | 12592954 | Cardiac disorder | |
125929541 | 12592954 | Cardiac flutter | |
125929541 | 12592954 | Chest pain | |
125929541 | 12592954 | Dizziness | |
125929541 | 12592954 | Drug administration error | |
125929541 | 12592954 | Dyspepsia | |
125929541 | 12592954 | Heart rate increased | |
125929541 | 12592954 | Heart rate irregular | |
125929541 | 12592954 | Osteoporosis | |
125929541 | 12592954 | Platelet count decreased | |
125929541 | 12592954 | Reverse tri-iodothyronine increased | |
125929541 | 12592954 | Tremor |
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 |
---|---|---|---|---|---|---|
125929541 | 12592954 | 1 | 2014 | 0 | ||
125929541 | 12592954 | 2 | 2010 | 2014 | 0 | |
125929541 | 12592954 | 3 | 201507 | 0 | ||
125929541 | 12592954 | 4 | 2015 | 0 | ||
125929541 | 12592954 | 5 | 2013 | 0 |