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Review: could Percocet cause Shortness of breath (Breathing difficulty)?

Summary: Shortness of breath is found among people who take Percocet, especially for people who are female, 60+ old, have been taking the drug for < 1 month, also take medication Zometa, and have Pain.

We study 24,313 people who have side effects while taking Percocet from FDA and social media. Among them, 2,139 have Shortness of breath. Find out below who they are, when they have Shortness of breath and more.

You are not alone: join a mobile support group for people who take Percocet and have Shortness of breath >>>

 

 

 

 

Percocet

Percocet has active ingredients of acetaminophen; oxycodone hydrochloride. It is often used in pain. (latest outcomes from 26,470 Percocet users)

Shortness of breath

Shortness of breath has been reported by people with high blood pressure, asthma, rheumatoid arthritis, pain, chronic obstructive pulmonary disease. (latest reports from 165,444 Shortness of breath patients)

On Feb, 12, 2015: 24,308 people reported to have side effects when taking Percocet. Among them, 2,139 people (8.80%) have Shortness Of Breath.

Trend of Shortness of breath in Percocet reports

Time on Percocet when people have Shortness of breath * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ years
Shortness of breath42.86%8.16%4.08%20.41%14.29%10.20%0.00%

Age of people who have Shortness of breath when taking Percocet * :

0-12-910-1920-2930-3940-4950-5960+
Shortness of breath0.00%0.11%1.79%4.76%10.18%19.00%24.26%39.90%

Severity of Shortness of breath when taking Percocet ** :

leastmoderateseveremost severe
Shortness of breath0.00%54.55%36.36%9.09%

How people recovered from Shortness of breath ** :

while on the drugafter off the drugnot yet
Shortness of breath0.00%0.00%100.00%

Top conditions involved for these people * :

  1. Pain (430 people, 20.10%)
  2. Metastases to bone (153 people, 7.15%)
  3. Multiple myeloma (145 people, 6.78%)
  4. Hypertension (136 people, 6.36%)
  5. Depression (123 people, 5.75%)

Top co-used drugs for these people * :

  1. Zometa (594 people, 27.77%)
  2. Aspirin (559 people, 26.13%)
  3. Oxycontin (445 people, 20.80%)
  4. Neurontin (423 people, 19.78%)
  5. Lasix (407 people, 19.03%)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Get connected: join our support group of percocet and shortness of breath on

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You may be interested at these reviews (Write a review):

  • Percocet and memory loss
    A close friend of mine has been using prescription Percocet for 5 to 6 years. Her MD first prescribed the lowest dosage possible to be taken 3 to 4 times daily for pain. I am aware that this medication frequently needs to be increased because it will become less effective. I don't know how many times he has increased the dosage but it has been many times. I believe now she is taking the highest dosage of it up to four to six times daily and six tablets at a time. I have made several attempts to tell her the information I know about Percocet and to have her to ask her MD about her now short and long term memory problems. Her response is to shout at me, telling me she needs that much for pain and to mind my own business when I tell her about the negative side effects I see, especially her daily and hourly memory problems. She has also said she has no reason to speak to her doctor about memory problems. I think that is because she fears he might lower the dosage. My concern about her poor memory only causes her to tell me I am the one with a bad memory, even though the only pain meds I infrequently take are OTC ones. According to my MD, I have been told my memory for my age of 63 is perfectly fine and better than most for my age. Also I take no medications with the side effects that cause memory problems. In addition when my MD prescribes new medication I always read the info that accompanies them, do research online and pay attention to all warnings and side effect info. The few times I have had side effects they have only been GI problems and I have consulted my MD regarding those and work with my MD for an alternative medication. My friend NEVER EVER reads any of the accompanying material that comes with her prescriptions. Also she never looks up her medications online to get additional information, including possible side effects. I worry about her very much and fear she now has an addiction to Percocet. Several years ago she asked her MD for Chantix to stop smoking, never reading the info supplied with the prescription. I urged to read the info and side effects. She declined, telling me she knew what she was doing. After two weeks of using Chantix she had a mental break down and ended up on the psych ward of our local hospital for 3 weeks. That medication was the first that began to cause her to have memory problems. She accepted that fact for about a month then dismissed it claiming her memory problems were over. They weren't because she was still taking Percocet. I understand no one wants to be told by a friend they suspect that person has memory problems, but I haven't done so to be mean or cruel, but only out of great love and concern. At this point with all the Percocet she takes daily she really is at a level to be considered an addict and I fear soon she will convince her MD to increase the dosage because it no longer controls her pain. I've written this review as a cautionary tale to inform others to be vigilant with their family, friends and loved ones as Percocet can and does cause short and long term memory loss. Although all my efforts to assist and speak to my friend have failed, please don't give up on those in your life who you notice are experiencing memory loss signs that take Percocet. If possible speak to them or their MD. Oh, and be prepared to be yelled at that you are the one with memory problems or to be told to mind your own business. And please, please read the information that accompanies all of your medications.
  • Faslodex driven hell
    I have metastatic breast cancer...which has spread to my bones. Needless to say...I'm not a happy camper. Faslodex was my oncologist’s drug of choice for me. I've been on it since July 28, 2014....My first month was loading dosage...and each month that has followed I receive two injections in my tush...250mg each...for a total of 500mg monthly. Tomorrow, Monday November 17, 2014, will be my third round...not including the month of loading. As per my PET scan one month ago...the Faslodex has not started working. From everything I have been told...and read...it takes four to even six rounds to start working...if in fact it works at all.....@%^&*@#...says it all...if ya know what I mean.

    What has kicked in from Faslodex...are some horrific side effects......About a month ago...I started having a strange little cough...dry...most of the time.....At times the cough becomes uncontrollable for aprox 15 / 20 minutes...then calms. NOTHING works at relieving it...although I suck down water like it is my last drink on earth...and use a wonderful...soothing throat drop, Halls Breezers...Cool Berry...which eases me...even if it is only psychologically, it is magical. The cough has gotten considerably worse over time...and for those that don't know me...I am sure they think I smoke ten packs a day. My voice is also affected at times due to the cough. My breathing is horrific...and I can no longer walk for any length of time...or for more than a short distance.....Nor can I walk and talk without coughing...and or losing my breath. Stamina...this I have none of!!! And this past week...the shit hit the fan.....Joining the cough...are bone and joint pains...as well as muscle pain. When I called my doctor...@ Sloan Kettering...I spoke with the nurse...and she had not a damn clue as to what might help. As a matter of fact...she told me that she has never heard of any of the side effects that I am now having. WHAT'S WRONG WITH THIS PICTURE???? EVERYTHING!!! However...when I check reputable sites...I find not a few...but hundreds of other people with the same side effects.

    From what I have read on all the sites...the only way "WE" are going to get help with issues like these...is by sharing with one another. Not one of the individuals that I speak of has had any positive help with their side effects from their doctors. Am I pissed off??? You bet I am. As for depression...that only comes in small doses for me.....like yesterday...when my body hurt me so badly...my cough was out of control...I had difficulty breathing...and I could not stand on my own two feet without holding on. That moment in time has passed...but for how long??? What will I be hit with next??? When???
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  • Which issue has caused my periodontitis, my fibromyalgia or spinal stenosis? (2 responses)
    At the age of 38 yrs old, I was diagnosed with Fibromyalgia and Spinal Stenosis. Obviously I had both of the disease for some years, and was struggling with the pain and symptoms for some time before I finally got checked, went through years being told they didn't find anything, told I had Herniated disks in My back only. Now with all the findings, there are 7 Herniated disks from My neck to My lower back.
    Also since 2010, I was diagnosed with Periodontitis and have been losing all of My teeth in the top of My mouth.
    I am 44 yrs old now, have been on disability for the last 4 years. I am down to 6 teeth in the top of My mouth, since having 1 removed just last week. They are telling Me that 3 more need to come out, and I am trying not to sink into total depression, especially since these are now My front teeth. I have a appointment today for a Denture Exam.

    I started researching today to see if this Periodontitis is related to either My Spinal Stenosis or My Fibromyalgia. Especially since I once again looked up the definition for Periodontitis. Which States;

    **Periodontal Disease and Bone Health. Periodontitis is a chronic infection that affects the gums and the bones that support the teeth. Bacteria and the body's own immune system break down the bone and connective tissue that hold teeth in place.

    Of course with My disease of Spinal Stenosis and the bone loss as well as the nerve narrowing, I thought the breaking down of the bone in the gums might have a connection. Research didnt find any linking.

    Now with Fibromyalgia, research showed 6 out of 17 thousand that they found. LOL Wow.. Well I guess I am "Number 7". Lucky Me! But it does make more sense now that looking at the definition. It is a Chronic infection (which Fibromyalia does create these) that effects the gums and bones. Bacteria and The Body's own Immune System break down the bone and connective tissue that hold the teeth. Which with Fibromyalgia, our Immune System is always all kinds of "Crazy"!

    Oh course you can not have any of these diseases, or any other health issues and wind up with Periodontitis. It happens. But I know from lots of reading, researching and living with Fibromyalgia, that it is "Very Possible"!

    I would sure like to know what others with these 2 diseases are experiencing.
    Have a Blessed Day.
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