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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 109540085 | 10954008 | 5 | F | 2000 | 20160812 | 20150325 | 20160821 | EXP | US-009507513-1201USA00122 | MERCK | 0.00 | M | Y | 0.00000 | 20160821 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 109540085 | 10954008 | 1 | PS | PROPECIA | FINASTERIDE | 1 | Oral | 1 MG, QD | Y | 20788 | 1 | MG | FILM-COATED TABLET | QD | |||||
| 109540085 | 10954008 | 2 | SS | LOVASTATIN. | LOVASTATIN | 1 | Oral | UNK, UNKNOWN | Y | 0 | TABLET | ||||||||
| 109540085 | 10954008 | 3 | SS | FLEXERIL | CYCLOBENZAPRINE HYDROCHLORIDE | 1 | Oral | UNK, UNKNOWN | Y | 0 | TABLET | ||||||||
| 109540085 | 10954008 | 4 | C | PAXIL | PAROXETINE HYDROCHLORIDE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 109540085 | 10954008 | 5 | C | CARVEDILOL. | CARVEDILOL | 1 | Unknown | UNK, UNKNOWN | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 109540085 | 10954008 | 1 | Alopecia |
| 109540085 | 10954008 | 2 | Product used for unknown indication |
| 109540085 | 10954008 | 3 | Product used for unknown indication |
| 109540085 | 10954008 | 4 | Depression |
| 109540085 | 10954008 | 5 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 109540085 | 10954008 | HO |
| 109540085 | 10954008 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 109540085 | 10954008 | Adverse event | |
| 109540085 | 10954008 | Alcohol abuse | |
| 109540085 | 10954008 | Anxiety | |
| 109540085 | 10954008 | Blood testosterone decreased | |
| 109540085 | 10954008 | Cognitive disorder | |
| 109540085 | 10954008 | Depression | |
| 109540085 | 10954008 | Diarrhoea | |
| 109540085 | 10954008 | Erectile dysfunction | |
| 109540085 | 10954008 | Fatigue | |
| 109540085 | 10954008 | Fibromyalgia | |
| 109540085 | 10954008 | Gastrooesophageal reflux disease | |
| 109540085 | 10954008 | Loss of libido | |
| 109540085 | 10954008 | Male orgasmic disorder | |
| 109540085 | 10954008 | Marital problem | |
| 109540085 | 10954008 | Otitis media | |
| 109540085 | 10954008 | Pain | |
| 109540085 | 10954008 | Pancreatic enzymes increased | |
| 109540085 | 10954008 | Pancreatitis | |
| 109540085 | 10954008 | Panic attack | |
| 109540085 | 10954008 | Post-traumatic stress disorder | |
| 109540085 | 10954008 | Quality of life decreased | |
| 109540085 | 10954008 | Self esteem decreased | |
| 109540085 | 10954008 | Serotonin syndrome | |
| 109540085 | 10954008 | Sexual dysfunction | |
| 109540085 | 10954008 | Sinusitis |
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 |
|---|---|---|---|---|---|---|
| 109540085 | 10954008 | 1 | 20000802 | 2011 | 0 | |
| 109540085 | 10954008 | 4 | 1991 | 0 | ||
| 109540085 | 10954008 | 5 | 1999 | 0 |