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rivastigmine

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Brand names: Exelon

Acetylcholinesterase Inhibitor Rx

Rivastigmine (Exelon) is a medicine that helps improve memory and thinking in people with dementia. It works by increasing a chemical in the brain that is important for these functions.

Drug Pricing (NADAC)

Brand Price

$21.97/unit

Generic Price

$0.16/unit

Generic Savings

99%

Generic Available

Yes (11 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

What it does

This medicine treats mild to moderate dementia caused by Alzheimer's disease.

Common side effects

Nausea, Vomiting, Loss of appetite

Key warnings

This medicine can cause significant nausea, vomiting, diarrhea, loss of appetite, and weight loss.

How It Works

Rivastigmine helps increase the amount of a chemical called acetylcholine in your brain. Acetylcholine is important for memory and thinking. By increasing this chemical, rivastigmine can help improve these functions in people with dementia.

How to Take It

Take rivastigmine capsules with food, in the morning and evening. For Alzheimer's, you'll likely start with 1.5 mg twice a day. Your doctor may increase the dose every 2 weeks to a maximum of 6 mg twice a day. For Parkinson's disease dementia, the dose may be increased every 4 weeks.

Pregnancy & Breastfeeding

It is not known if rivastigmine will harm an unborn baby. Talk to your doctor if you are pregnant or plan to become pregnant. It is also not known if rivastigmine passes into breast milk. Talk to your doctor about the best way to feed your baby if you are taking this medicine.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and continue with your regular schedule.

Storage

Store rivastigmine capsules at room temperature, away from moisture and heat.

Side Effects (from patient reports)

Based on 11,242 FDA adverse event reports.

Death
2,176
Fall
1,664
Seeing or hearing things that are not there
1,365
Confusion
1,258
The medicine is not working
896
Throwing up
883
Feeling sick to your stomach
826
Feeling lightheaded
771
Trouble walking
713
Lung infection
690

FDA Adverse Event Report Analysis

Detailed analysis of 17,976 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2000–2025.

Total Reports

17,976

Death-Related Reports

4,544

Hospitalization Reports

6,537

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 8,646 (51%)
Male 8,286 (49%)

Age Distribution

0–17 53
18–44 39
45–64 734
65–74 2,514
75+ 7,025

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 DEATH 2,177
2 FALL 1,664
3 HALLUCINATION 1,365
4 CONFUSIONAL STATE 1,258
5 DRUG INEFFECTIVE 896
6 VOMITING 885
7 NAUSEA 827
8 DIZZINESS 771
9 GAIT DISTURBANCE 713
10 PNEUMONIA 690
11 MALAISE 648
12 SOMNOLENCE 646
13 DIARRHOEA 640
14 FATIGUE 637
15 URINARY TRACT INFECTION 610

Reactions in Death Reports

DEATH 2,177
PNEUMONIA 348
FALL 238
GENERAL PHYSICAL HEALTH DETERIORATION 183
PARKINSON^S DISEASE 178
CEREBROVASCULAR ACCIDENT 165
CARDIAC ARREST 164
HALLUCINATION 141
DEMENTIA 136
DYSPHAGIA 134

Reactions in Hospitalization Reports

FALL 1,004
CONFUSIONAL STATE 554
PNEUMONIA 475
HALLUCINATION 457
URINARY TRACT INFECTION 435
VOMITING 426
NAUSEA 339
GENERAL PHYSICAL HEALTH DETERIORATION 324
ASTHENIA 320
DIARRHOEA 294

Source: FDA FAERS (Adverse Event Reporting System) FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Serious Warnings

This medicine can cause significant nausea, vomiting, diarrhea, loss of appetite, and weight loss. These side effects can lead to dehydration, which can be serious. If you have a skin reaction that spreads, stop taking this medicine.

Known Drug Interactions

7 DRUG INTERACTIONS Concomitant use with metoclopramide, beta-blockers, or cholinomimetic and anticholinergic drugs is not recommended (7.1, 7.2, 7.3) 7.1 Metoclopramide Due to the risk of additive extrapyramidal adverse reactions, the concomitant use of metoclopramide and rivastigmine tartrate is not recommended.

Mechanism: Both drugs can cause similar side effects related to muscle control and movement. Taking them together increases the risk of developing shaky movements or muscle stiffness.

What to do: This combination is not recommended. Talk to your doctor about alternative treatments to avoid these movement-related side effects.

7.3 Beta-blockers Additive bradycardic effects resulting in syncope may occur when rivastigmine tartrate is used concomitantly with beta-blockers, especially cardioselective beta-blockers (including atenolol).

Mechanism: Both of these medicines can slow your heart rate. Taking them at the same time might cause your heart to beat too slowly or make you faint.

What to do: Watch for dizziness or fainting and have your doctor check your heart rate regularly.

7.2 Cholinomimetic and Anticholinergic Medications Rivastigmine tartrate may increase the cholinergic effects of other cholinomimetic medications and may also interfere with the activity of anticholinergic medications (e.g., oxybutynin, tolterodine).

Mechanism: These drugs have opposite effects on the body. Rivastigmine can prevent oxybutynin from working the way it is supposed to.

What to do: Tell your doctor if your symptoms return, as they may need to change your medications.

7.2 Cholinomimetic and Anticholinergic Medications Rivastigmine tartrate may increase the cholinergic effects of other cholinomimetic medications and may also interfere with the activity of anticholinergic medications (e.g., oxybutynin, tolterodine).

Mechanism: Rivastigmine works against drugs like tolterodine. This means tolterodine might not work as well when taken with rivastigmine.

What to do: Your healthcare provider should monitor how well your medications are working and adjust them if needed.

Common Questions

What should I do if I feel sick to my stomach after taking this medicine?
Talk to your doctor. They may lower your dose or suggest ways to manage the nausea.
Can I take this medicine with other medicines?
Tell your doctor about all the medicines you take, including over-the-counter drugs and supplements.
How long will I need to take this medicine?
Your doctor will decide how long you need to take rivastigmine.
What happens if I stop taking rivastigmine?
Talk to your doctor before stopping rivastigmine. Your symptoms may worsen if you stop suddenly.
Will this medicine cure my dementia?
No, rivastigmine does not cure dementia, but it may help improve your symptoms.
Can I drive while taking this medicine?
Rivastigmine can cause dizziness or sleepiness. Be careful driving or operating machinery until you know how this medicine affects you.
What if I accidentally take too much rivastigmine?
Call your doctor or go to the nearest emergency room right away.
Are there any foods I should avoid while taking this medicine?
There are no specific foods to avoid, but it's best to take it with meals to reduce stomach upset.
How long does it take for this medicine to start working?
It may take several weeks to notice the full effects of rivastigmine.
Can my family member give me this medication even if I forget?
Yes, it is important that a caregiver helps you remember to take this medication as prescribed.
What are the common side effects of rivastigmine?
The most commonly reported side effects of rivastigmine include Nausea, Vomiting, Loss of appetite, Upset stomach, Weakness. Based on 11,242 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
Does rivastigmine interact with other medications?
Yes, rivastigmine has 4 known drug interactions. Notable interactions include metoclopramide, atenolol, oxybutynin. Always inform your doctor about all medications you are taking.
What drug class is rivastigmine?
rivastigmine belongs to the Acetylcholinesterase Inhibitor drug class. It requires a prescription (Rx). This medicine treats mild to moderate dementia caused by Alzheimer's disease.
Is there a generic version of rivastigmine?
Yes, generic rivastigmine is available from 11 manufacturers. The generic costs $0.16 per unit compared to $21.97 for the brand version, saving approximately 99%. Pricing is based on NADAC (National Average Drug Acquisition Cost) data from CMS.
Is rivastigmine safe during pregnancy?
It is not known if rivastigmine will harm an unborn baby. Talk to your doctor if you are pregnant or plan to become pregnant. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.

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What the FDA Data Shows for rivastigmine

The FDA label for rivastigmine (sold under brand names such as Exelon) classifies it as a prescription-only medication in the Acetylcholinesterase Inhibitor class. This medicine treats mild to moderate dementia caused by Alzheimer's disease. Official labeling lists 5 commonly reported side effects, including Nausea, Vomiting, Loss of appetite.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 11,242 voluntary reports. The database also lists 4 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated moderate severity. NADAC pricing from CMS shows a generic unit cost of $0.16 versus $21.97 for the brand — a 99% generic savings.

Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history, and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.

Last updated: March 21, 2022

All federal data sources used on this page