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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126116161 | 12611616 | 1 | I | 20160722 | 20160801 | 20160801 | EXP | CA-PURDUE PHARMA-CAN-2016-0006926 | PURDUE | 37.00 | YR | Y | 122.00000 | KG | 20160726 | CN | CA | CA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126116161 | 12611616 | 1 | PS | METHYLPHENIDATE HYDROCHLORIDE. | METHYLPHENIDATE HYDROCHLORIDE | 1 | Unknown | UNK | U | 205831 | |||||||||
126116161 | 12611616 | 2 | SS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | 10 MG, UNK | U | 0 | 10 | MG | TABLET | ||||||
126116161 | 12611616 | 3 | SS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | 5 MG, UNK | U | 0 | 5 | MG | TABLET | ||||||
126116161 | 12611616 | 4 | SS | CLONAZEPAM. | CLONAZEPAM | 1 | Unknown | UNK | U | 0 | TABLET | ||||||||
126116161 | 12611616 | 5 | SS | ESOMEPRAZOLE | ESOMEPRAZOLE | 1 | Unknown | UNK | U | 0 | |||||||||
126116161 | 12611616 | 6 | SS | FENTANYL. | FENTANYL | 1 | Unknown | UNK | U | 0 | |||||||||
126116161 | 12611616 | 7 | SS | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 | TABLET | ||||||||
126116161 | 12611616 | 8 | SS | METHADONE | METHADONE HYDROCHLORIDE | 1 | Unknown | UNK | U | U | 0 | ||||||||
126116161 | 12611616 | 9 | SS | SERTRALINE | SERTRALINE HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 | CAPSULE | ||||||||
126116161 | 12611616 | 10 | SS | BUDESONIDE W/FORMOTEROL FUMARATE | BUDESONIDEFORMOTEROL FUMARATE | 1 | Unknown | UNK | U | U | 0 | ||||||||
126116161 | 12611616 | 11 | SS | VALSARTAN AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDEVALSARTAN | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126116161 | 12611616 | 1 | Product used for unknown indication |
126116161 | 12611616 | 2 | Product used for unknown indication |
126116161 | 12611616 | 4 | Product used for unknown indication |
126116161 | 12611616 | 5 | Product used for unknown indication |
126116161 | 12611616 | 6 | Product used for unknown indication |
126116161 | 12611616 | 7 | Product used for unknown indication |
126116161 | 12611616 | 8 | Product used for unknown indication |
126116161 | 12611616 | 9 | Product used for unknown indication |
126116161 | 12611616 | 10 | Product used for unknown indication |
126116161 | 12611616 | 11 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126116161 | 12611616 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126116161 | 12611616 | Drug level increased | |
126116161 | 12611616 | Overdose | |
126116161 | 12611616 | Unresponsive to stimuli |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |