Pharm
Pramlintide
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Pramlintide
, Symlin, SymlinPen, Amylinomimetic, Amylin Analogue
See Also
Type II Diabetes Medications
Indications
Type I and II
Diabetes Mellitus
Adjunct to
Insulin
therapy
Third-line measure due to
Hypoglycemia
risk and cost
Contraindications
Gastroparesis
Hypoglycemia
history (esp. if patient unaware of episodes)
Mechanism
Pramlintide is a synthetic analogue of human Amylin
Amylin is secreted with
Insulin
from the
Pancreas
Amylin lowers post-prandial
Blood Sugar
s
Delays gastric emptying
Inhibits
Glucagon
release
Precautions
Switch to new pen device which replaces the vials and prevents dosing errors
Warning: Pen concentration is different than vial concentration
Dosing errors are common with the vials
Dosing is typically listed in mcg, but is drawn up in
Insulin
syringes marked with units
A patient who mistakes their 30 mcg dose for 30 units is accidentally taking 180 mcg
Medications
Pramlintide (SymlinPen) 1000 mcg/ml pen injector: 1.5 or 2.7 ml
Pen replaces the older vials that required a 100 unit 0.3 ml syringe
Store unopened vials in refrigerator
Once opened, may be kept at room
Temperature
for up to 28 days
Dosing
Protocol
Reduce short and mixed-acting
Insulin
dose by 50%
Take with at least 250 calories (>30 g
Carbohydrate
)
Inject SQ into
Abdomen
or thigh
Type I Diabetes Mellitus
Start: 15 mcg (2.5 U) SQ three times daily immediately before meals
Titrated in 15 mcg increments every 3-7 days if tolerated (without significant
Nausea
,
Vomiting
)
Target: 30 to 60 mcg (5-10 units) SQ three times daily before meals
Discontinue or lower dose to 30 mcg if significant
Nausea
Type II Diabetes Mellitus
Start: 60 mcg (10 U) SQ three times daily immediately before meals
Target: 60 to 120 mcg (10-20 units) SQ three times daily before meals
Discontinue or lower dose to 60 mcg if significant
Nausea
Adverse effects
Nausea
(28%) or
Vomiting
(8%): Especically Type I DM (related to
Delayed Gastric Emptying
)
Contraindicated in
Gastroparesis
Headache
(13%)
Anorexia
(9%)
Abdominal Pain
(8%)
Severe
Hypoglycemia
(4.7%)
Occurs 3 hours after
Insulin
and Pramlintide dose (higher risk in
Type 1 Diabetes Mellitus
)
FDA Black box warning (decrease
Insulin
dose before starting)
Safety
Pregnancy Category C
Unknown safety in
Lactation
Efficacy
Drops
Hemoglobin A1C
0.5 to 0.6% (contrast with
Placebo
: 0.25% )
No good longterm outcome data (other agents with better longterm efficacy are preferred)
Lowers weight 3 lb or 1.4 kg (
Placebo
: 0.6 kg gained)
Drug Interactions
Gastrointestinal motility medications
Avoid with Pramlintide
Alpha glucosidase Inhibitors
Avoid with Pramlintide
Drugs that require rapid onset
Take rapid onset medications 1 hour prior to, or 2 hours after Pramlintide
Resources
Pramlintide (DailyMed)
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4aea30ff-eb0d-45c1-b114-3127966328ff
References
Jones (2007) Am Fam Physician 75:1831-5 [PubMed]
Kruger (2004) Drugs 64: 1419-32 [PubMed]
Kleppinger (2003) Ann Pharmacother 37:1082-9 [PubMed]
Ryan (2005) Clin Ther 27:1500-12 [PubMed]
Steinberg (2019) Am Fam Physician 99(4): 237-43 [PubMed]
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