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Gabapentin, Percocet for a 57-year old woman





Summary: 690 female patients aged 57 (±5) who take the same drugs are studied.

This is a personalized study for a 57 year old female patient who has Neuropathic Pain, Pain. The study is created by eHealthMe based on reports from FDA and social media.

What are the drugs

Gabapentin has active ingredients of gabapentin. It is often used in neuralgia. (latest outcomes from Gabapentin 39,518 users)

Percocet has active ingredients of acetaminophen; oxycodone hydrochloride. It is often used in pain. (latest outcomes from Percocet 26,450 users)

What are the conditions

Neuropathic pain (pain due to nerve inflammation and damage) can be treated by Gabapentin, Lyrica, Neurontin, Cymbalta, Amitriptyline Hydrochloride. (latest reports from Neuropathic Pain 978 patients)

Pain can be treated by Hydrocodone Bitartrate And Acetaminophen, Vicodin, Percocet, Tramadol Hydrochloride, Ibuprofen, Lortab. (latest reports from Pain 280,210 patients)

On Nov, 23, 2014: 690 females aged 53 (±5) who take Gabapentin, Percocet are studied

Gabapentin, Percocet outcomes

Information of the patient in this study:

Age: 53

Gender: female

Conditions: Neuropathic Pain, Pain

Drugs taking:
- Gabapentin - 100MG (gabapentin): used for < 1 month
- Percocet - 325MG;5MG (acetaminophen; oxycodone hydrochloride): used for < 1 month

eHealthMe real world results:

Drug effectiveness over time :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ yearsnot specified
Gabapentin is effective66.67%
(2 of 3 people)
50.00%
(1 of 2 people)
100.00%
(1 of 1 people)
n/a0.00%
(0 of 2 people)
33.33%
(1 of 3 people)
0.00%
(0 of 1 people)
n/a
Percocet is effective100.00%
(1 of 1 people)
0.00%
(0 of 3 people)
n/a100.00%
(1 of 1 people)
50.00%
(2 of 4 people)
100.00%
(1 of 1 people)
n/a0.00%
(0 of 1 people)

Most common drug interactions over time * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ yearsnot specified
Nausea (feeling of having an urge to vomit)DiarrhoeaDiverticular Perforation (serious gastrointestinal condition in which the intestine's walls are perforated)Insomnia Exacerbated (severe sleeplessness)Arthralgia (joint pain)Cerebrovascular Accident (sudden death of some brain cells due to lack of oxygen when the blood flow to the brain is impaired by blockage or rupture)Nausea (feeling of having an urge to vomit)Pain
PainAbdominal DiscomfortDiverticulitis (digestive disease which involves the formation of pouches (diverticula) within the bowel wall)Aggression AggravatedMood Swings (an extreme or rapid change in mood)Hypoaesthesia (reduced sense of touch or sensation)Hot Flashes (sudden feelings of heat)Nausea (feeling of having an urge to vomit)
Gastroenteritis (inflammation of stomach and intestine)Dyspepsia (indigestion)Sepsis (a severe blood infection that can lead to organ failure and death)Hallucinations, Mixed (sensations that appear real but are created by your mind -mixed)Back PainAnaemia (lack of blood)Anxiety
FallHeadache (pain in head)Abdominal PainParanoia Aggravated (serious psychotic disorder characterized by delusions of persecution with or without grandeur)Suicidal IdeationSwellingOedema Peripheral (superficial swelling)
Blood Glucose IncreasedTremor (trembling or shaking movements in one or more parts of your body)Mania Aggravated (worse irritable mood)AnxietyDehydration (dryness resulting from the removal of water)Back Pain
Pruritus (severe itching of the skin)Nausea (feeling of having an urge to vomit)AngerHypokalaemia (low potassium)Fatigue (feeling of tiredness)
Upper Limb FractureSleep Phase Rhythm Disturbance (heart rate disturbances during sleep)Drug DependenceMyocardial Infarction (destruction of heart tissue resulting from obstruction of the blood supply to the heart muscle)Paraesthesia (sensation of tingling, tickling, prickling, pricking, or burning of a person's skin with no apparent long-term physical effect)
Thrombocytopenia (decrease of platelets in blood)Neuropathic Pain (pain due to nerve inflammation and damage)DepressionHyperlipidaemia (presence of excess lipids in the blood)Dyspnoea (difficult or laboured respiration)
Renal Tubular Necrosis (death of kidney tubules)Sleeplessness (a sleep disorder in which there is an inability to fall asleep or to stay asleep as long as desired)Affect Lability (emotional incontinence)Pain In ExtremityOsteonecrosis Of Jaw (death of bone of jaw)
Feeling AbnormalOedema Peripheral (superficial swelling)Polysubstance AbuseWeight DecreasedAnaemia (lack of blood)

* Some reports may have incomplete information.

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.

You can also:

You are not alone! Join a related mobile support group:
- support group for people who have Neuropathic Pain
- support group for people who have Pain
- support group for people who take Gabapentin
- support group for people who take Percocet

Can you answer these questions (Ask a question):

More questions for: Neuropathic Pain, Pain

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.
  • 3 strong drugs together against neuropathic pain
    Neuropathic pain debuted when I was 24, now I'm 50. Received diagnosed with Ehler-Danlos syndrome (EDS), joint hypermobility type, when I was 35 years old. So it can take some time to get a diagnose. And as EDS-patient I do not belong to any clinic. Orthopedics says that EDS is not orthopedic, rheumatology says that EDS is not an autoimmune disease, GPs say that EDS is too difficult, and so on. Sooner or later we all end up at Psychiatry, even if we are not depressed.

    The first kind of pain I got when I was 24 came from low back, but I experienced as pelvic pain and leg pain. It was clearly a neuropathic pain, but it took years to find out. Later it was treated by a pain clinic with cortisone around the genitofemoral nerves (both sides). Since this treatment didn't result in lasting freedom from pain, the pain clinic started to give me RF (radio frequency) treatment. This made the pain disappeared after one year, and I was 80% free from it between 2002 and 2014, 12 years. The pain doctors said pain could return after 10 years.

    The other kind of neuropathic pain started 2003 with intense stomach pain. During 6 months I could hardly eat nothing due to nausea and vomiting. After this 6 months, stomach pain changed to almost unbearable pain in upper back.
    What happened 2003, and what all the doctors missed, was that the right lowest ribs slid up over the sternum. This rib dislocation is till there today, but now with a lot of cartilage formed around the rib where it is stuck in the lower end of the sternum. The dislocation is clearly visible on X-ray. This has greatly affected the thoracic spine. I have a scoliosis which I had not before 2003. And I still have severe pain in the thoracic spine.

    It was initially treated with morphine daily, and later with Durogesic (fentanyl), but this didn't help much. 2005 I was hospitalized because I had too much pain to take care of myself and my hygiene. After some months the doctors started to give me clonazepam because the muscles along the spine was in a chronic seizures. Clonazepam helped, but I could still have a lot of pain in two vertebrae in the thoracic spine. It felt as if someone drilled into the vertebrae without anesthesia. After a few months, doctors also prescribed me methadone. Then the pain disappeared almost completely. Since 2006, I have eaten clonazepam and methadone every day, and I need to sleep in an armchair to not get more pain because of moving during sleep.

    There are side effects. After 1,5 years with clonazepam and methadone I started to have panic attacks. Or rather one long panic attack which didn't stop before I got treatment with amitryptilin and pregabalin (Lyrica). These 2 medicines stopped the panic disorder completely after some hours, and the panic was then gone. Then I got side effects of these 2 medicines, amitryptilin & Lyrica, too. I gained a lot of weight (from 83 to 148 kg) and got much water (edema) in both my legs under the knees and in both feet. The feet could swallow to the double size. 2012 I stopped with amitryptilin and started to loose weight again (in Aug 2014 below 80 kg) and get less water in my legs. Today I eat as little medicines I can, but I have to take methadone, clonazepam and Lyrica every day, twice. If I try to take away one of these 3 medicines, I got pain problems at once. Lyrica is the most painful one to take away. In Sept-Dec 2013 I lowered Lyrica from 300 mg daily, to 150, then to 75 and finally 0 mg. The pain I had was extremely difficult to handle. It didn't help to take more methadone or anything else. I have checked on Internet and found that many people got pain from quitting with Lyrica. Most people start eating it again. So did I. But 2006 and 2007 it was enough to treat the pain with methadone and clonazepam, I got the Lyrica against anxiety not pain. But today I take Lyrica against pain.

    Beside weight gain and leg edema, clonazepam and Lyrica significantly affect the sexual desire. And Lyrica alone makes it almost impossible to ejaculate. All four drugs together (clonazepam, methadone, amitryptiline and Lyrica), make one forget all about sex life. You don't even miss it. When I stopped with amitryptiline and lowered Lyrica (still taking clonazepam and methadone), I could suddenly easily get erections again, feel desire, but not getting orgasms. This is quite difficult to deal with.

    The pain pattern is greatly affected, by pain and by the medicines. So is the mood. I get something which feels like heavy depression, especially if I take the medicines late that day. I should take a medicine like methadone 3 times a day, because the effects of the tablet lasts around 8 hours. But I take them every 12 hours, to have a low consumption in case doctors prescribe them too late (which happens, and then it's good to have a spouse going to the pharmacy buying them for you, because you have too much pain to go yourself).

    Since methadone is also used for treating heroine addicts, medical staff treat you with disrespect when they see that it says "methadone" in your health record. I need to show a certificate that says that I deal with chronic neuropathic pain, that I never have had problems with drug addiction, to get normal respect.

    I wanted to share this because I think I am alone in the world with these medicines in combination against neuropathic pain caused by hypermobile joints, joint dislocation and muscle spasms. After trying almost everything else, including surgery cutting nerves, methadone, clonazepam and Lyrica seems to be the only way to kill my pain. But it's a life where you always is questioned, because of the use of methadone. I can guarantee that everybody in the world should accept these medicines if they had experienced the unbearable pain I had in upper back before they started to give me clonazepam and methadone.
  • Ranexa and erectile dysfunction
    I have experienced moderate ED with taking multiple heart and NO meds. This has been manageable and acceptable. Cardiologist added Ranexa (Ranalozine) 3 weeks ago and I am now experiencing complete erectile and ejaculatory failure.
  • Cough and gabapentin
    Have chronic cough for 6 yr's at least.3 yr's ago it got bad enough to seek doc. Help. Took all the tests . Tried to tell me I had asthma,copd, ect. Put me on sprivia, symbicort, singular, helped a little for awhile. Long story short. Went to one doc. He asked me some questions about my cough. Figured out it usually started with a tickle on the left side of my throat. And he put me on gabapentin 300mg. 3 times Aday. Which is for nerve damage. It took about 7days to see some change. And about 35days To stop the chronic cough. I still cough once in awhile. But no chronic coughing. Now I am going to try and see if I can stop the other med,s one at a time and see what happens
  • Had nms in 2005, will trileptal increase chance of recurrence?
    In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.

More reviews for: Neuropathic Pain, Pain

Comments from related studies:

  • From this study (5 months ago):

  • I've been diagnosed with sero-negative rheumatoid arthritis. I have only tested minimally positive on the anti-CCP test and had a slightly high SED rate. My most recent tests showed some slight elevation in some RA marker tests, but nothing really significant. My rheumatologist is now doubting whether I have RA or some other pain syndrome going on.

    Reply

    IHateRA on Jul, 22, 2014:

    My first RA Dr. put me on Plaquenil, it seemed to work for six months, then stopped - I thought the dose would be adjusted but it wasn't, so I went to another RA Doc - C-RP wasn't too high, sero neg. Was put on methotrexate - I ended up with a mouth sore the NEXT day, then bumps started appearing on my face, like zits, but NOT zits. I didn't touch them, but they ulcerated, left me full of scars on face, legs, etc - I have been OFF methotrexate for 5 years AND still have the same problem along with a daily fever (100+) and severe sweating - I knew the bumps were a sign of being allergic to Methotrexate, I quit it right away, called Dr. to get in - they told me 3 months (I was an established patient). In terms of fever and sweating, the ONLY thing I have in common with some of these posts and drug lists is METHOTREXATE - I wouldn't allow a pet to take it. I seem to have more in common with a friend who as MS - but my reg. doc doesn't listen to that. I can't take bio. drugs (live in "fungal" region), so I take pain medicine - as little as possible, I guess the Methotrexate is STILL messing with my body. I have a very good acupuncturist - when I told him that my Doc. wasn't "sure" about RA, he poked me (lightly) with his finger in two places and ask which hurt more. He confirmed the RA as it travels on certain meridians in Chinese medicine. Had I picked a different spot for hurting more, then we would have to figure out what I really had. My joints are deteriorating but now I'm afraid of the drugs for RA, so I just put up with and manage the pain (which is extreme) with pain meds, cold therapy (I love my cryo-cuff), and acupuncture. I wish that the side effects of RA drugs weren't as bad as they are! Leaving Cymbalta, Lyrica, Plaquenil and Methotrexate (all at different times) OUT of my body made me realize that they did affect me - I was "foggy" and sluggish mentally but didn't really notice it until I quit them.

    Reply

  • From this study (7 months ago):

  • Taking xarelto after knee surgery yesterday. Foot is now swollen on that leg and would like to know if I can take the bumetanide while taking xarelto.

    Reply

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NOTE: The study is based on active ingredients. Other drugs that have the same active ingredients are also considered.

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