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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125694741 | 12569474 | 1 | I | 20160628 | 20160707 | 20160719 | 20160719 | EXP | GB-MHRA-TPP23157515C2987890YC1467107322792 | GB-TEVA-676405ACC | TEVA | 82.00 | YR | M | Y | 58.00000 | KG | 20160719 | MD | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125694741 | 12569474 | 1 | PS | SIMVASTATIN. | SIMVASTATIN | 1 | U | U | 76052 | 80 | MG | ||||||||
| 125694741 | 12569474 | 2 | C | ATORVASTATIN | ATORVASTATIN | 1 | 1 DOSAGE FORMS DAILY; AT NIGHT. | 1 | DF | 0 | 1 | DF | TABLET | QD | |||||
| 125694741 | 12569474 | 3 | C | DERMOL | BENZALKONIUM CHLORIDECHLORHEXIDINE HYDROCHLORIDEISOPROPYL MYRISTATEPARAFFIN | 1 | 2 DOSAGE FORMS DAILY; ON AFFECTED AREAS | 52 | DF | 0 | 1 | DF | BID | ||||||
| 125694741 | 12569474 | 4 | C | DORZOLAMIDE HYDROCHLORIDE. | DORZOLAMIDE HYDROCHLORIDE | 1 | 2 GTT DAILY; | 1149.91666 | Gtt | 0 | 1 | GTT | BID | ||||||
| 125694741 | 12569474 | 5 | C | FUSIDIC ACID | FUSIDIC ACID | 1 | APPLY SMALL VOLUME TO AFFECTED SITES TWICE A DAY | 0 | |||||||||||
| 125694741 | 12569474 | 6 | C | NASEPTIN | CHLORHEXIDINE HYDROCHLORIDENEOMYCIN SULFATE | 1 | 8 DOSAGE FORMS DAILY; APPLY INSIDE BOTH NOSTRILS | 8 | DF | 0 | 2 | DF | QID | ||||||
| 125694741 | 12569474 | 7 | C | TAMSULOSIN HYDROCHLORIDE. | TAMSULOSIN HYDROCHLORIDE | 1 | 1 DOSAGE FORMS DAILY; | 414 | DF | 0 | 1 | DF | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125694741 | 12569474 | 2 | Blood cholesterol increased |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125694741 | 12569474 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125694741 | 12569474 | Abnormal dreams | |
| 125694741 | 12569474 | Myalgia | |
| 125694741 | 12569474 | Pain in extremity |
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 |
|---|---|---|---|---|---|---|
| 125694741 | 12569474 | 1 | 20141201 | 0 | ||
| 125694741 | 12569474 | 2 | 20160628 | 0 | ||
| 125694741 | 12569474 | 3 | 20160602 | 0 | ||
| 125694741 | 12569474 | 4 | 20141201 | 0 | ||
| 125694741 | 12569474 | 5 | 20160505 | 20160506 | 0 | |
| 125694741 | 12569474 | 6 | 20160628 | 0 | ||
| 125694741 | 12569474 | 7 | 20150511 | 0 |