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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127595201 | 12759520 | 1 | I | 20160724 | 20160905 | 20160919 | 20160919 | EXP | FR-PFIZER INC-2016418649 | PFIZER | 80.00 | YR | F | Y | 45.00000 | KG | 20160919 | MD | FR | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127595201 | 12759520 | 1 | PS | SUNITINIB MALATE. | SUNITINIB MALATE | 1 | Oral | 50 MG, UNK | Y | N | 21938 | 50 | MG | ||||||
127595201 | 12759520 | 2 | C | CO-APROVEL | HYDROCHLOROTHIAZIDEIRBESARTAN | 1 | Oral | 300 MG, DAILY | 0 | 300 | MG | ||||||||
127595201 | 12759520 | 3 | C | KEPPRA | LEVETIRACETAM | 1 | Oral | 250 MG, DAILY | 0 | 250 | MG | ||||||||
127595201 | 12759520 | 4 | C | OROCAL VITAMINE D3 /00278001/ | 2 | Oral | 500 MG, DAILY | 0 | 500 | MG | |||||||||
127595201 | 12759520 | 5 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Oral | 1000 MG, DAILY | 0 | 1000 | MG | ||||||||
127595201 | 12759520 | 6 | C | PARACETAMOL | ACETAMINOPHEN | 1 | 0 | ||||||||||||
127595201 | 12759520 | 7 | C | PIZOTIFENE | 2 | Oral | 0.5 MG, DAILY | 0 | .5 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127595201 | 12759520 | 1 | Metastatic renal cell carcinoma |
127595201 | 12759520 | 2 | Hypertension |
127595201 | 12759520 | 3 | Epilepsy |
127595201 | 12759520 | 4 | Osteoporosis |
127595201 | 12759520 | 5 | Pain |
127595201 | 12759520 | 6 | Prophylaxis |
127595201 | 12759520 | 7 | Headache |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127595201 | 12759520 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127595201 | 12759520 | Diarrhoea | |
127595201 | 12759520 | Escherichia urinary tract infection | |
127595201 | 12759520 | Fatigue | |
127595201 | 12759520 | Headache | |
127595201 | 12759520 | Malaise | |
127595201 | 12759520 | Vomiting |
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 |
---|---|---|---|---|---|---|
127595201 | 12759520 | 1 | 20160413 | 20160727 | 0 | |
127595201 | 12759520 | 3 | 20160418 | 0 |