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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118287792 | 11828779 | 2 | F | 200007 | 20160827 | 20151211 | 20160829 | EXP | FR-BRISTOL-MYERS SQUIBB COMPANY-10709350 | BRISTOL MYERS SQUIBB | 0.01 | YR | M | Y | 3.11000 | KG | 20160829 | OT | US | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
118287792 | 11828779 | 1 | PS | ZERIT | STAVUDINE | 1 | Transplacental | 80 MG, QD | U | 20412 | 80 | MG | CAPSULE, HARD | QD | |||||
118287792 | 11828779 | 2 | SS | ZERIT | STAVUDINE | 1 | Oral | UNK | U | 0 | ORAL SOLUTION | ||||||||
118287792 | 11828779 | 3 | SS | EPIVIR | LAMIVUDINE | 1 | Transplacental | 300 MG, QD | U | 0 | 300 | MG | QD | ||||||
118287792 | 11828779 | 4 | SS | RETROVIR | ZIDOVUDINE | 1 | Transplacental | 1 DF, UNK | U | 0 | 1 | DF | |||||||
118287792 | 11828779 | 5 | C | I RON | FERROUS FUMARATE | 1 | Transplacental | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
118287792 | 11828779 | 1 | Product used for unknown indication |
118287792 | 11828779 | 2 | Antiretroviral therapy |
118287792 | 11828779 | 3 | Product used for unknown indication |
118287792 | 11828779 | 4 | Product used for unknown indication |
118287792 | 11828779 | 5 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
118287792 | 11828779 | HO |
118287792 | 11828779 | CA |
118287792 | 11828779 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
118287792 | 11828779 | Anaemia macrocytic | |
118287792 | 11828779 | Foetal exposure during pregnancy | |
118287792 | 11828779 | Hypertriglyceridaemia | |
118287792 | 11828779 | Neutropenia | |
118287792 | 11828779 | Sickle cell anaemia |
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 |
---|---|---|---|---|---|---|
118287792 | 11828779 | 1 | 20000707 | 0 | ||
118287792 | 11828779 | 2 | 20000707 | 20000804 | 0 | |
118287792 | 11828779 | 5 | 20000707 | 0 |