Review: could Neurontin cause Arthrofibrosis?
Summary: Arthrofibrosis is reported only by a few people who take Neurontin.
We study 56,298 people who have side effects while taking Neurontin from FDA and social media. Find out below who they are, when they have Arthrofibrosis and more.
You are not alone: join a support group for people who take Neurontin and have Arthrofibrosis >>>
Neurontin has active ingredients of gabapentin. It is often used in neuralgia. (latest outcomes from 57,802 Neurontin users)
Arthrofibrosis (serious condition that can afflict knee joints that have either been recently injured, operated upon, or both) has been reported by people with osteoporosis, osteopenia, birth control, high blood pressure, angiogram abnormal. (latest reports from 66 Arthrofibrosis patients)
On Mar, 27, 2015: 56,293 people reported to have side effects when taking Neurontin. Among them, 1 people (0.00%) has Arthrofibrosis.
Time on Neurontin when people have Arthrofibrosis * :
Age of people who have Arthrofibrosis when taking Neurontin * :
Severity of Arthrofibrosis when taking Neurontin ** :
How people recovered from Arthrofibrosis ** :
Top conditions involved for these people * :
- Knee arthroplasty (1 people, 100.00%)
Top co-used drugs for these people * :
- Prevacid (1 people, 100.00%)
- Flexeril (1 people, 100.00%)
- Wellbutrin (1 people, 100.00%)
- Avandia (1 people, 100.00%)
- Elavil (1 people, 100.00%)
* 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.
Do you have Arthrofibrosis while taking Neurontin?
You are not alone! Join a support group on :
- support group for people who take Neurontin and have Arthrofibrosis
- support group for people who take Neurontin
- support group for people who have Arthrofibrosis
Drugs in real world that are associated with:
Could your condition cause:
- A study of drug interactions between Magnesium, Calcium, Vitamin D, Restasis, Gabapentin, Remeron, Buspar, Naproxen for a 54-year old woman with General Symptom, Eyes - Dry, Restless Leg Syndrome, Ptsd, Generalised Anxiety Disorder, Arthritis - Osteoarthritis. The patient has Anxiety Postoperative
- A study of drug interactions between Calcium, Krill Oil, Aspirin, Lisinopril, Lipitor, Metformin, Gabapentin, Tecfidera for a 56-year old woman with Bone Health, Ms, Heart Health, Blood Pressure - Aging Changes, Blood Cholesterol Abnormal, Type 2 Diabetes Mellitus, Neurological Pain.
- A study of side effects of Gabapentin for a 68-year old man with Neuropathy. The patient has Inflammation
- A study of side effects of Gabapentin for a 60-year old woman with Neuropathy.
- A study of drug interactions between Neurontin, Mobic for a 31-year old man with Spinal Cord Compression. The patient has Nerve Pain
Recent Neurontin related drug comparison:
- Comparions of Neurontin, Zyprexa, Wellbutrin Xl, Latuda, Risperidone for a 38-year old man who has Schizoaffective Disorder
- Comparions of Omeprazole, Phentermine, Zorvolex, Gabapentin for a 49-year old woman who has Nerve Pain
- Comparions of Fentanyl, Gabapentin for a 65-year old woman who has Myelitis Transverse
- Comparions of Gabapentin, Metformin Hydrochloride for a 40-year old woman who has Polycystic Ovarian Syndrome (PCOS)
- Comparions of Gabapentin, Amlodipine, Olmetec for a 72-year old woman who has High Blood Pressure
NOTE: The study is based on active ingredients and brand name. Other drugs that have the same active ingredients (e.g. generic drugs) are NOT considered.
WARNING: Please DO NOT STOP MEDICATIONS without first consulting a physician since doing so could be hazardous to your health.
DISCLAIMER: All material available on eHealthMe.com is for informational purposes only, and is not a substitute for medical advice, diagnosis, or treatment provided by a qualified healthcare provider. All information is observation-only, and has not been supported by scientific studies or clinical trials unless otherwise stated. Different individuals may respond to medication in different ways. Every effort has been made to ensure that all information is accurate, up-to-date, and complete, but no guarantee is made to that effect. The use of the eHealthMe site and its content is at your own risk.
You may report adverse side effects to the FDA at http://www.fda.gov/medwatch/ or 1-800-FDA-1088 (1-800-332-1088).
If you use this eHealthMe study on publication, please acknowledge it with a citation: study title, URL, accessed date.