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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126590711 | 12659071 | 1 | I | 20160809 | 20160816 | 20160816 | PER | PHEH2016US020315 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160816 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126590711 | 12659071 | 1 | PS | RITALIN LA | METHYLPHENIDATE HYDROCHLORIDE | 1 | Oral | 40 MG, BID | U | UNKNOWN | 21284 | 40 | MG | EXTENDED RELEASE CAPSULES | BID | ||||
126590711 | 12659071 | 2 | SS | RITALIN | METHYLPHENIDATE HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 | |||||||||
126590711 | 12659071 | 3 | SS | METHYLPHENIDATE HYDROCHLORIDE. | METHYLPHENIDATE HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 | |||||||||
126590711 | 12659071 | 4 | SS | ANTIDEPRESSANTS | UNSPECIFIED INGREDIENT | 1 | Unknown | UNK | U | 0 | |||||||||
126590711 | 12659071 | 5 | C | OTHER MINERAL SUPPLEMENTS | MINERALS | 1 | Unknown | UNK | U | 0 | |||||||||
126590711 | 12659071 | 6 | C | RITALIN - SLOW RELEASE | 2 | Unknown | UNK | U | 0 | ||||||||||
126590711 | 12659071 | 7 | C | VITAMINS | VITAMINS | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126590711 | 12659071 | 1 | Product used for unknown indication |
126590711 | 12659071 | 2 | Product used for unknown indication |
126590711 | 12659071 | 3 | Product used for unknown indication |
126590711 | 12659071 | 4 | Product used for unknown indication |
126590711 | 12659071 | 5 | Product used for unknown indication |
126590711 | 12659071 | 6 | Product used for unknown indication |
126590711 | 12659071 | 7 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126590711 | 12659071 | Confusional state | |
126590711 | 12659071 | Drug ineffective | |
126590711 | 12659071 | Drug intolerance | |
126590711 | 12659071 | Headache |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |