Would you have Upset stomach (Nausea and vomiting) when you have Hepatitis c?
Summary: Upset stomach is found among people with Hepatitis c, especially people who are female, 50-59 old, also have High blood pressure, and take medication Ribavirin. We study 2,477 people who have Upset stomach (Nausea and vomiting) and Hepatitis c from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
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Hepatitis c can be treated by Ribavirin, Peginterferon, Pegasys, Incivek. (latest reports from 41,477 Hepatitis C patients)
Upset stomach has been reported by people with high blood pressure, pain, type 2 diabetes, depression, rheumatoid arthritis. (latest reports from 142,502 Upset stomach patients)
On May, 22, 2015: 2,390 people who have hepatitis c and Upset Stomach are studied.
Gender of people who have hepatitis c and experienced Upset stomach * :
|Upset stomach||60.63%||39.37% |
Age of people who have hepatitis c and experienced Upset stomach * :
|Upset stomach||0.04%||0.41%||0.19%||2.80%||9.21%||27.73%||41.36%||18.26% |
Severity of the symptom * :
|least||moderate||severe||most severe |
|Upset stomach||0.00%||100.00%||0.00%||0.00% |
Top co-existing conditions for these people * :
- Hypertension (215 people, 9.00%)
- Depression (167 people, 6.99%)
- Pain (134 people, 5.61%)
- Anxiety (88 people, 3.68%)
- Diabetes mellitus (67 people, 2.80%)
- Insomnia (58 people, 2.43%)
- Gastrooesophageal reflux disease (51 people, 2.13%)
- Hiv infection (44 people, 1.84%)
- Hypothyroidism (42 people, 1.76%)
- Prophylaxis (42 people, 1.76%)
Most common drugs used by these people * :
- Ribavirin (2,390 people, 100.00%)
- Peg-intron (2,372 people, 99.25%)
- Pegasys (1,775 people, 74.27%)
- Rebetol (1,176 people, 49.21%)
- Incivek (995 people, 41.63%)
- Copegus (677 people, 28.33%)
- Ribasphere (541 people, 22.64%)
- Victrelis (213 people, 8.91%)
- Effexor (158 people, 6.61%)
- Zoloft (149 people, 6.23%)
* Approximation only. 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.
Get connected: join our support group of hepatitis c and upset stomach on
Do you have Hepatitis C and Upset Stomach?
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Comments from related studies:
From this study (2 weeks ago):
had every gastro test, had gall bladder surgery, been to endocrinologist; many many blood tests; noone can figure this out. Been going on for over 6 months. Desperate
From this study (2 weeks ago):
I was diagnosed after a routine diabetes checkup with my PCP, who is a specialist in internal medicine. He referred me to a urologist, who confirmed the kidney stones. The urologist prescribed ciprofloxin and tamsulosin. At the same time, my PCP prescribed farxiga to help control my A1c. About 10 days later, I started breaking out in a rash with very large, painful wheals on my legs, arms, neck and buttocks. I first day my PCP, since this is also an adverse side effect of Farxiga, as listed on their PI sheet. I was taken off Farxiga, and issued resolved itself for a few days. 3 days later, this same rash recurred. I called the urologist. Since I ran out of my prescription of ciprofloxin, it was concluded that the tamsulosin was the issue. The urologist stopped the dosage, but never made any notes on my chart regarding this reaction.
The urologist also decided the my kidney stones were too large to dissolve with medication, and I was referred to the surgeon on staff in this practice. We discussed the options for surgery, and I opted for laser lithotripsy. The surgeon then prescribed tamsulosin, as well as urocit-k, since further bloodwork from the lab showed I had a low potassium level, as well as low creatinine levels. This occurred 1 week before my surgery, after having a cystoscope exam. The rash returned with the large wheals on my arms and legs, as well as my buttocks. When I reported to the hospital for surgery, the nurse commented on the condition of my legs. I did not say anything, as the anesthesia was beginning to take effect. The stones were removed, and a stent was placed in my bladder.
8 days after the surgery, and I still was not feeling well, not having any type of appetite. I started noticing several, small red dots appearing over 80% of my body. I drove myself to the nearest emergency room. The attending physician ran some tests, and determined I was having a severe reaction to tamsulosin and urocit-k. I was taken off both prescriptions, and prescribed vistaril and famotidine and was sent home.
I was still not recovering very well, and was getting weaker. Roughly 1 week after my visit to the ER, I had the stent removed, and I notified this surgeon, IN NO UNCERTAIN TERMS, that I made a visit to the ER with a severe reaction to tamsulosin and Urocit-K. It was then I found out the urologist NEVER made a note on my record about the tamsulosin allergy.
4 days after that incident, I got up, went to the bathroom, and discovered blood in my stool. This caused my to call 911, and requested the ambulance to transport me to the ER where I was previously admitted. I was admitted to ICU, and my PCP partner, who as in the same group practice as my PCP, ordered a colonoscopy, as soon as I was stable and could be released from ICU. The colonoscopy was performed, and the gastroenterologist determined it was definitely ischemic colitis, caused by the adverse reaction to tamsulosin and urocit-k
From this study (4 weeks ago):
I hope this finds everyone feeling like I do at least a bit, slightly better than the way we all felt before joining eHealth.com I know it helps me just to talk about my problems with people in the same boat and I get a positive feeling on occasion when I learn more about my problems and feel good in that I am not just sitting around bumming out all day. I at least get satisfaction that I am doing something to help myself and my loved ones who worry about me. It gives me a reason to motor on when I keep in mind how many people have been helped by social media and live Reality TV shows like The Doctors.
After completing a very difficult Hep-C treatment including several emergencies caused by the Hep-C medications lowering my White Blood Cell Count I managed a positive outcome identified in August of 2013, ridding myself of the Hep-C Disease. Six (6) monthly blood tests were conducted post Hep-C treatment to check for any re-infection. None was detected. During my last blood test visit in January of 2014 I was told I am Hep-C Free but the blood tests revealed I had very Low Testosterone and Hypothyroidism which could be causing my major fatigue problem.
Note: A couple of weeks after my first blood test check back in July/August 2014 my hair started falling out and thinning almost daily. After about 3 months it stopped and my hair actually grew back to normal. This was the ONLY positive drug related problem that got better with time.
About 6 months Post Hep-C treatment I began feeling majorly fatigued. I spent almost all of 2014 with doctors trying to diagnose my condition(s) and develop a treatment plan. First the doctors went after the Low-T problem. They got my numbers in order with injections but no change in my fatigue level. Next was the Hypothyroidism. I was given one injection that was supposed to have noticeable effect after 3 days I think. Again my numbers were good but no change in my fatigue problem. The doctor basically gave up on me and told me to pursue seeing a doctor for the many allergies I have which he said can cause fatigue or to wait and hope the Hep-C medication induced the problem and maybe it will go away after the Hep-C medication completely leaves my system which I was told can take up to 18 months and in some case longer.
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