Miscellaneous metabolic agents
What are Miscellaneous metabolic agents?
List of Miscellaneous metabolic agents
View by Brand | Generic
| Drug Name | Avg. Rating | Reviews |
|---|---|---|
| pegvaliase systemic (Pro) |
1 review | |
| miglustat systemic (Pro) |
1 review | |
| eliglustat systemic (Pro) |
1 review | |
| vutrisiran systemic (Pro) | No reviews | |
| uridine systemic (Pro) | No reviews | |
| sapropterin systemic (Pro) | No reviews | |
| resmetirom systemic | No reviews | |
| patisiran systemic (Pro) | No reviews | |
| nitisinone systemic (Pro) | No reviews | |
| nedosiran systemic (Pro) | No reviews | |
| mitapivat systemic (Pro) | No reviews | |
| migalastat systemic (Pro) | No reviews | |
| metreleptin systemic (Pro) | No reviews | |
| lumasiran systemic (Pro) | No reviews | |
| lonafarnib systemic (Pro) | No reviews | |
| inotersen systemic (Pro) | No reviews | |
| givosiran systemic (Pro) | No reviews | |
| fosdenopterin systemic (Pro) | No reviews | |
| eplontersen systemic (Pro) | No reviews | |
| burosumab systemic (Pro) | No reviews | |
| asfotase alfa systemic (Pro) | No reviews | |
| For ratings, users were asked how effective they found the medicine while considering positive/adverse effects and ease of use (1 = not effective, 10 = most effective). | ||
See also
Medical conditions treated or associated with miscellaneous metabolic agents:
- Capecitabine Overdose
- Fabry Disease
- Familial Hypophosphatemia
- Fluorouracil Overdose
- Gaucher Disease
- Hereditary Amyloidosis
- Hereditary Orotic Aciduria
- Hereditary Tyrosinemia Type 1
- Hutchinson-Gilford Syndrome
- Hypophosphatasia
- Lipodystrophy
- Molybdenum Cofactor Deficiency Type A
- Nonalcoholic Steatohepatitis
- Osteomalacia
- Phenylketonuria
- Pompe Disease
- Porphyria
- Primary Hyperoxaluria
- Transthyretin-Related Amyloidosis
- X-Linked Hypophosphatemia
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
