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Galantamine Hydrobromide

Popular Brands: : Reminyl, Galantamine Hydrobromide, Galantamine, Razadyne, Razadyne Er
Official FDA Reports13,472
Social Media Events36
Total Posts68
Avg. Review Score3.01/ 5
Active Ingredients
  • Galantamine Hydrobromide
Approved Uses *

* Extracted from Drug Label

Manufacturers
  • American Health Packaging
  • Barr Laboratories Inc
  • Janssen Pharmaceuticals Inc
  • Roxane Laboratories, Inc

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Reminyl.

* Extracted from FDA Adverse Event Report

Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (FAERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


The proportion of people completing user reviews who complained about a side effect.

The proportion of social media adverse event complaints for each adverse event type.

The proportion of FAERS (FDA) adverse event complaints for each adverse event type.


Galantamine Hydrobromide Side Effects

  Social Media
(Online Comments)
FAERS
(Reports Submitted to FDA)
Side Effect On Drug
Label
Overall
Alarm
Reports % of
Reports
Alarm Reports % of
Reports
Alarm

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


User Voices

The following are comments from users that experienced side effects while taking Galantamine Hydrobromide

Agitation

... Family felt she did not need the medication and the dosage was decreased dramatically. In two days the client's behaviors have increased. Refusing cares and increased agitation . Sometimes we don't ...


Source: Razadyne oral : User Ratings covering ...

View full report on Galantamine Hydrobromide related agitation

Did the author experience agitation while taking razadyne?

What is this?

Nausea

The quality of my life has changed dramatically as this treatment has caused severe stomach pain, nausea and diahrea as well as wakefullness and agitation in the evening. I am requesting my Dr. to ta...


Source: Razadyne oral : User Ratings covering ...

View full report on Galantamine Hydrobromide related nausea

Did the author experience nausea while taking razadyne?

What is this?

Malaise

... in the evening. I am requesting my Dr. to take me off as the side effects are very severe... I would rather suffer the consequences of Alzheimer disease then live by feeling sick with severe flu symp...


Source: Razadyne oral : User Ratings covering ...

View full report on Galantamine Hydrobromide related malaise

Did the author experience malaise while taking razadyne?

What is this?

Tell us about your Experience with Galantamine Hydrobromide

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: None

Posted By Anonymous in drugs.com on June 4, 2011 @ 12:00 am

Reminds me of Adderall but only a natural way to acquire the same or a similar effect. I am in the process of speaking with my grandmothers doctor to see if she can take it for her Alzheimer's.

Druginformer Identified Side Effects: None

Posted By Anonymous in fdb.rxlist.com on February 5, 2011 @ 12:00 am

M

Druginformer Identified Side Effects: None

Posted By Anonymous in drugs.com on September 24, 2010 @ 12:00 am

My husband is 69 and has been diagnosed with Alzheimer's and dementia. He started this medication about two weeks ago. He is already showing signs of improvement. He is able to read and comprehend ...

Druginformer Identified Side Effects: Agitation

Posted By whirlwind in fdb.rxlist.com on August 8, 2010 @ 12:00 am

... Family felt she did not need the medication and the dosage was decreased dramatically. In two days the client's behaviors have increased. Refusing cares and increased agitation. Sometimes we don't ...

Druginformer Identified Side Effects: Malaise, Nausea, Abdominal discomfort, Agitation, Influenza, Diarrhoea

Posted By Anonymous in fdb.rxlist.com on July 16, 2010 @ 12:00 am

... in the evening. I am requesting my Dr. to take me off as the side effects are very severe... I would rather suffer the consequences of Alzheimer disease then live by feeling sick with severe flu symp...

Druginformer Identified Side Effects: Confusional state, Abnormal dreams, Headache, Nausea, Nightmare

Posted By Beaux in fdb.rxlist.com on February 15, 2010 @ 12:00 am

ad dreams, nightmares, headaches, and nausea. Feel more confused with than without.

Druginformer Identified Side Effects: None

Posted By Anonymous in drugs.com on January 24, 2010 @ 12:00 am

My 81 yr old dad has been on it for 4 months and there's been a marked improvement in function and mood and alertness. Memory improvement is small but he's improved much. He's not like a zombie anymo...

Druginformer Identified Side Effects: Dizziness, Nausea, Somnolence

Posted By nan in fdb.rxlist.com on October 28, 2009 @ 12:00 am

Severe nausea,dizziness and fatigue.Inability to function normally. Impaired cognition which improved after stopping the meddication.

Druginformer Identified Side Effects: None

Posted By hracklin in fdb.rxlist.com on September 16, 2009 @ 12:00 am

Druginformer Identified Side Effects: None

Posted By Anonymous in fdb.rxlist.com on June 2, 2009 @ 12:00 am

IREGULAR HEAT BEAT.


Additional Drug Information


* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.