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Recently Prescribed Co~careldopa Have Experienced Excessive Sweating During The Night

A MyParkinsonsTeam Member asked a question 💭
spilsby

have been diagnosed for pd 10 yrs med ,pipexus and rasagline problems with night sweating after co careldopa was added

March 10, 2024
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Side Effects of Parkinson’s Disease Treatment Read Article...
MyParkinsonsTeam

Excessive sweating can be a side effect of Co-Careldopa (Levodopa/Carbidopa). Here are some key points to consider:

- Common Side Effects: Sweating, dizziness, drowsiness, nervousness, headaches, confusion, memory problems, nightmares, problems sleeping, loss of appetite, or changes in the sense of taste
- Serious Side Show Full Answer

Excessive sweating can be a side effect of Co-Careldopa (Levodopa/Carbidopa). Here are some key points to consider:

- Common Side Effects: Sweating, dizziness, drowsiness, nervousness, headaches, confusion, memory problems, nightmares, problems sleeping, loss of appetite, or changes in the sense of taste.
- Serious Side Effects: Inform your doctor immediately if you experience a fast, pounding heartbeat, hallucinations, suicidal thoughts, depression, increased urge to have sex or gamble, stools containing blood or a tarry substance, vomit containing blood or a substance resembling coffee grounds, hoarseness, or abnormal body movements.
- Darkened Fluids: The medication may cause your urine, sweat, or saliva to turn dark colors, which can stain clothes.

If the excessive sweating becomes bothersome or severe, it's important to discuss this with your doctor.

September 6, 2024
Hi, this is just a check-in, based on a phrase you mentioned. If you — or anyone else who sees this — is thinking about self-harm, we want to say that you are an important part of this community. No part of this is easy, but there is support that can help. Read more >
A MyParkinsonsTeam Member

Started experiencing night sweats also, terrible wake up with body cold yet feeling wet from sweat,so afraid I smell,use anti persistent,perfume, deodorant, everything I can get my hands on, really disturbs my sleep and confidence!!!!

March 13, 2024
A MyParkinsonsTeam Member

Wow...me too!

March 10, 2024

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