AMLODIPINE\LISINOPRIL: 71 Adverse Event Reports & Safety Profile
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71
Total FAERS Reports
0
Deaths Reported
34
Hospitalizations
71
As Primary/Secondary Suspect
1
Life-Threatening
Active Ingredient: AMLODIPINE BESYLATE\LISINOPRIL ·
First Report: 20171208 · Latest Report: 20221201
What Are the Most Common AMLODIPINE\LISINOPRIL Side Effects?
#1 Most Reported
Bradycardia
31 reports (43.7%)
#2 Most Reported
Nocturia
28 reports (39.4%)
#3 Most Reported
Insomnia
28 reports (39.4%)
All AMLODIPINE\LISINOPRIL Side Effects by Frequency
| Side Effect | Reports | % of Total | Deaths | Hosp. |
|---|---|---|---|---|
| Bradycardia | 31 | 43.7% | 0 | 5 |
| Hypoaesthesia | 28 | 39.4% | 0 | 2 |
| Insomnia | 28 | 39.4% | 0 | 2 |
| Nocturia | 28 | 39.4% | 0 | 2 |
| Memory impairment | 27 | 38.0% | 0 | 0 |
| Pain | 27 | 38.0% | 0 | 0 |
| Anxiety | 26 | 36.6% | 0 | 0 |
| Ataxia | 26 | 36.6% | 0 | 0 |
| Balance disorder | 26 | 36.6% | 0 | 0 |
| Central nervous system lesion | 26 | 36.6% | 0 | 0 |
| Dizziness | 26 | 36.6% | 0 | 0 |
| Dysarthria | 26 | 36.6% | 0 | 0 |
| Erectile dysfunction | 26 | 36.6% | 0 | 0 |
| Fall | 26 | 36.6% | 0 | 0 |
| Gait spastic | 26 | 36.6% | 0 | 0 |
| Hypertonic bladder | 26 | 36.6% | 0 | 0 |
| Micturition urgency | 26 | 36.6% | 0 | 0 |
| Monoparesis | 26 | 36.6% | 0 | 0 |
| Movement disorder | 26 | 36.6% | 0 | 0 |
| Multiple sclerosis relapse | 26 | 36.6% | 0 | 0 |
Who Reports AMLODIPINE\LISINOPRIL Side Effects? Age & Gender Data
Gender: 24.7% female, 75.3% male. Average age: 54.5 years. Most reports from: CA. View detailed demographics →
Is AMLODIPINE\LISINOPRIL Getting Safer? Reports by Year
| Year | Reports | Deaths | Hosp. |
|---|---|---|---|
| 2017 | 1 | 0 | 0 |
| 2019 | 3 | 0 | 0 |
| 2020 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 0 |
What Is AMLODIPINE\LISINOPRIL Used For?
| Indication | Reports |
|---|---|
| Secondary progressive multiple sclerosis | 25 |
| Hypertension | 20 |
| Atrial fibrillation | 15 |
| Product used for unknown indication | 10 |
Official FDA Label for AMLODIPINE\LISINOPRIL
Official prescribing information from the FDA-approved drug label.