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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124683393 | 12468339 | 3 | F | 20160601 | 20160826 | 20160615 | 20160831 | EXP | US-PFIZER INC-2016291980 | PFIZER | 58.00 | YR | M | Y | 100.00000 | KG | 20160831 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124683393 | 12468339 | 1 | PS | Genotropin MQ | SOMATROPIN | 1 | 0.2 MG, 1X/DAY (IN THE EVENING) | Y | M77206 | 20280 | .2 | MG | POWDER FOR SOLUTION FOR INJECTION | QD | |||||
| 124683393 | 12468339 | 2 | SS | Genotropin MQ | SOMATROPIN | 1 | Y | 20280 | POWDER FOR SOLUTION FOR INJECTION | ||||||||||
| 124683393 | 12468339 | 3 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 20 MG, 1X/DAY | 0 | 20 | MG | QD | |||||||
| 124683393 | 12468339 | 4 | C | TRICOR | FENOFIBRATE | 1 | Oral | 145 MG, ALTERNATE DAY (EVERY OTHER DAY) | 0 | 145 | MG | QOD | |||||||
| 124683393 | 12468339 | 5 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 2000 IU, 1X/DAY | 0 | 2000 | IU | QD | |||||||
| 124683393 | 12468339 | 6 | C | MAGNESIUM | MAGNESIUM | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124683393 | 12468339 | 1 | Growth hormone deficiency |
| 124683393 | 12468339 | 2 | Empty sella syndrome |
| 124683393 | 12468339 | 3 | Blood cholesterol increased |
| 124683393 | 12468339 | 4 | Blood cholesterol increased |
| 124683393 | 12468339 | 5 | Vitamin D decreased |
| 124683393 | 12468339 | 6 | Blood magnesium decreased |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124683393 | 12468339 | HO |
| 124683393 | 12468339 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124683393 | 12468339 | Blood pressure increased | |
| 124683393 | 12468339 | Cold sweat | |
| 124683393 | 12468339 | Dizziness | |
| 124683393 | 12468339 | Ear discomfort | |
| 124683393 | 12468339 | Tinnitus |
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 |
|---|---|---|---|---|---|---|
| 124683393 | 12468339 | 1 | 20160601 | 0 |