Review: could Ventolin hfa cause Loss of voice (Hoarseness or changing voice)?
Summary: Loss of voice is reported only by a few people who take Ventolin hfa.
We study 247 people who have side effects while taking Ventolin hfa from FDA and social media. Find out below who they are, when they have Loss of voice and more.
You are not alone: join a mobile support group for people who take Ventolin hfa and have Loss of voice >>>
Ventolin hfa has active ingredients of albuterol sulfate. It is often used in asthma. (latest outcomes from 359 Ventolin hfa users)
Loss of voice
Loss of voice has been reported by people with asthma, chronic obstructive pulmonary disease, high blood pressure, osteoporosis, rheumatoid arthritis. (latest reports from 14,355 Loss of voice patients)
On Jan, 20, 2015: 247 people reported to have side effects when taking Ventolin hfa. Among them, 1 people (0.40%) has Loss Of Voice.
Time on Ventolin hfa when people have Loss of voice * :
Gender of people who have Loss of voice when taking Ventolin hfa * :
|Loss of voice||100.00%||0.00% |
Age of people who have Loss of voice when taking Ventolin hfa * :
|Loss of voice||0.00%||0.00%||0.00%||0.00%||0.00%||0.00%||0.00%||100.00% |
Severity of Loss of voice when taking Ventolin hfa ** :
How people recovered from Loss of voice ** :
Top conditions involved for these people * :
- Asthma (1 people, 100.00%)
Top co-used drugs for these people * :
- Cozaar (1 people, 100.00%)
- Proventil (1 people, 100.00%)
- Catapres (1 people, 100.00%)
- Actonel (1 people, 100.00%)
- Albuterol (1 people, 100.00%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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Do you have Loss Of Voice while taking Ventolin Hfa?
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- support group for people who take Ventolin hfa and have Loss Of Voice
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- support group for people who have Loss Of Voice
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I started taking Plavix prior to a stent placement one week ago. After two or three days I developed a hoarseness and voice interference.
- Is it my thyroid or am i mentally ill? diagnosed w/ hashimoto's thyroiditis but untreated - chronic pain unmanaged also (2 answers)
I moved to OR from HI and brought all my records, signed releases, and had many diagnoses, all but the thyroid, was being treated and long-term. I also took Oxycontin & Oxycodone for severe chronic pain from bilateral SI joint fusion (right screw protrudes & leg also becomes numb and weak with activity) & lumbar and cervical degeneration & facet arthropathy. I had volunteered reducing dosage as I'm always trying to reduce Rx intake to alleviate side effects (I am tiny, even for a youth & adult dosages seem to drug me). Next month, it was known that I could not function well because pain was not managed, but needed to resolve it in OR, as moving. OR Drs. refused to return me to higher dosage (taking minimalist Oxycontin 10 mg CR & Oxycodone/Acet 5mg). After being unable to get up to go to bathroom, walk, contacted adult services to see about in home services & possible foster care placement for young son since I was losing independence & failing in general health & cognitive functioning. I was forced to take bottles of OTC Tylenol to function, with Dr's knowledge, & knowing I had past lesions on liver to follow. Several months later had follow up liver ultrasound, & new small lesions found on liver. After emailing dr about from DHS questioning failure to manage my pain vs. conditions that were disabiling, 6 months later, dr told me I was experiencing withdrawals every morning & finally agreed to increase Oxycontin to 15 mg, which has enabled me to tolerate the pain & function. I have been treated as a drug-seeking patient since attempting to transfer my care.
I have multiple autoimmune conditions, most of which I no longer treat with Rx as I have been overmedicated & side effects are too numerous. So I actually am opposite in many ways. I stopped Lyrica, Silenor (sleep), Elmiron, Bentyl, Dexilant. Stress affects me seriously since I had a TBI and experience anxiety stress disorder, which seems to contribute to auto immune responses. But still knew triggers & familiar with self - this thyroid diagnosis & symptoms experienced new & too destabilizing to live.
Diagnosed w/ Hashimoto's thyroiditis after 1/2 thyroid removed Nov 2011; my antibodies are unbelievably high. I declined in thinking, memory, anxiety-unable to think/track, losing most,getting lost driving, sleep very dysfunctional, too emotional, crying easily & often (unusual for me). I feared losing ability to live independently. My maintenance Rx (Silenor, Lyrica) seemed to drug me. I tried to explain to drs. that I needed thyroid replacement hormones that I never had these problems before.
They referred me to a psychiatrist for medicine management consultation, who gave me mental health diagnoses (histrionic personality disorder, somatoform (hypochondria) that discredited me & ruined my medical records for future validity. Is it thyroid symptoms? Was unmanaged pain contributing? Too much Tylenol? What does a dysfunctional thyroid do to a person? How do I get my medical record addressed to reflect accuracy?
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i ran out of adderall,i want to use albuterol instead in my cocktail of oxycodone ir and xanax,will it feel anything close to adderal or rittlin??
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Comments from related studies:
From this study (2 years ago):
Jennifer on Mar, 15, 2013:
I am a 29yr old female n my gyno told me about Provella probiotic, so I took it for 28 days n developed a massive infection. The ER doc said it was because it changed my Flora too fast or I could have immune health probs (autoimmune). I wish gyno would have warned me n have had problems since. Make sure u check side effects n interactions. Wish I did, had to have surgery, laproscopy n cystscopy bc I was still having severe pains n female organ region. Docs r suppose to make u better not worse, Becareful b 4 taking any new drug!
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