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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127613751 | 12761375 | 1 | I | 20140910 | 20160920 | 20160920 | EXP | IT-GLENMARK PHARMACEUTICALS INC, USA.-2014GMK011204 | GLENMARK | 14.00 | YR | F | Y | 0.00000 | 20160920 | OT | IT | IT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127613751 | 12761375 | 1 | PS | VERAPAMIL | VERAPAMIL HYDROCHLORIDE | 1 | Unknown | 1 MG/KG, QD | 78906 | 1 | MG/KG | ||||||||
127613751 | 12761375 | 2 | I | VERAPAMIL | VERAPAMIL HYDROCHLORIDE | 1 | Unknown | 1.5 MG/KG, QD (TITRATED IN A PERIOD OF 14 DAYS) | 78906 | 1.5 | MG/KG | ||||||||
127613751 | 12761375 | 3 | I | VERAPAMIL | VERAPAMIL HYDROCHLORIDE | 1 | Unknown | UNK, MAINTENANCE PERIOD | 78906 | ||||||||||
127613751 | 12761375 | 4 | I | PHENYTOIN. | PHENYTOIN | 1 | Unknown | UNK | U | 0 | |||||||||
127613751 | 12761375 | 5 | C | TOPIRAMATE. | TOPIRAMATE | 1 | Unknown | UNK | 0 | ||||||||||
127613751 | 12761375 | 6 | C | ETOSUXIMIDA | 2 | Unknown | UNK | 0 | |||||||||||
127613751 | 12761375 | 7 | C | VALPROIC ACID. | VALPROIC ACID | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127613751 | 12761375 | 2 | Severe myoclonic epilepsy of infancy |
127613751 | 12761375 | 4 | Epilepsy |
127613751 | 12761375 | 5 | Epilepsy |
127613751 | 12761375 | 6 | Epilepsy |
127613751 | 12761375 | 7 | Epilepsy |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127613751 | 12761375 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127613751 | 12761375 | Drug interaction | |
127613751 | 12761375 | Product use issue | |
127613751 | 12761375 | Seizure |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |