Listril Side Effects


Common Listril Side Effects

The most commonly reported Listril side effects (click to view or check a box to report):

Paranoia (1)
Rhabdomyolysis (1)
Type Ii Hypersensitivity (1)
No Therapeutic Response (1)
Hallucination (1)
Aortic Stenosis (1)
B-cell Lymphoma Stage Iv (1)
Fall (1)
Angioedema (1)

If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Listril Side Effects Reported to FDA

Listril Side Effect Report#8029324-6
B-cell Lymphoma Stage Iv
This is a report of a 57-year-old male patient (weight: NA) from Switzerland, suffering from the following health symptoms/conditions: hypertensive heart disease,type 2 diabetes mellitus, who was treated with Listril (dosage: 20 Mg, Qd, start time:
Jan 01, 2005), combined with:
  • Byetta (Ch20120100151310 Ug, Bid)
  • Atacand (32 Mg, Qd)
  • Aspirin (Unk)
  • Metformin Hcl (1 G, Qd)
  • Carvedilol (50 Mg, Qd)
  • Amlodipine Besylate (Unk)
and developed a serious reaction and side effect(s): B-cell Lymphoma Stage Iv after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Listril treatment in male patients, resulting in B-cell Lymphoma Stage Iv side effect. The patient was hospitalized.
Listril Side Effect Report#5268981-4
Hallucination, Paranoia
This report suggests a potential Listril (ngx) (lisinopril) Tablets, 5mg Hallucination side effect(s) that can have serious consequences. A 42-year-old male patient (weight: NA) from Switzerland was diagnosed with the following symptoms/conditions: NA and used Listril (ngx) (lisinopril) Tablets, 5mg (dosage: 5 Mg, Qd, Oral) starting
Nov 23, 2006. After starting Listril (ngx) (lisinopril) Tablets, 5mg the patient began experiencing various side effects, including: Hallucination, ParanoiaAdditional drugs used concurrently:
  • Keppra (750 Mg, Bid, Oral)
  • Lorazepam (5 Mg, Qd, Oral)
  • Prazine /net/ (promazine Hydrochloride) (100 Mg, Qd, Oral)
  • Subutex (1 Mg, Qd, Oral)
  • Dormicum Roche (midazolam Maleate) (30 Mg, Qd, Oral)
  • Rohypnol (flunitrazepam) Film-coated Tablet, 1mg (1 Mg, Qd, Oral)
  • Beloc Zok (metoprolol Succinate) Tablet (50 Mg, Qd, Oral)
  • Plavix
Although Listril (ngx) (lisinopril) Tablets, 5mg demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Hallucination, may still occur.
Listril Side Effect Report#5268972-3
Angioedema, Aortic Stenosis, Fall, No Therapeutic Response, Rhabdomyolysis, Type Ii Hypersensitivity
This Angioedema problem was reported by a physician from Switzerland. A 77-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: secondary hypertension,staphylococcal infection,aortic valve stenosis. On
Jan 31, 2007 this consumer started treatment with Listril (ngx) (lisinopril) Tablets, 20mg (dosage: 20 Mg, Qd, Oral). The following drugs were being taken at the same time:
  • Floxacillin Sodium (1 G, Qid, Intravenous)
  • Aspirin Cardio (acetylsalicylic Acid) Film-coated Tablet, 100mg (100 Mg, Qd, Oral)
  • Clexane (enoxaparin Sodium, Heparin-fraction, Sodium Salt) Vial, 100mg (80 Mg, Qd, Subcutaneous)
  • Simvastatin (20 Mg, Qd, Oral)
  • Nexium (20 Mg, Qd, Oral)
  • Lantus (insulin Glargine) Vial, 100 Iu
  • Beloc (metoprolol Tartrate) Tablet
  • Dafalgan (paracetamol) Effervescent Tablet, 500 Mg
When using Listril (ngx) (lisinopril) Tablets, 20mg, the patient experienced the following unwanted symptoms/side effects: Angioedema, Aortic Stenosis, Fall, No Therapeutic Response, Rhabdomyolysis, Type Ii HypersensitivityThe patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Angioedema, may become evident only after a product is in use by the general population.

The appearance of Listril on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.

What are common Listril Side Effects for Women?

Women Side EffectsReports
Angioedema 1
Aortic Stenosis 1
Fall 1
No Therapeutic Response 1
Rhabdomyolysis 1
Type Ii Hypersensitivity 1

What are common Listril Side Effects for Men?

Men Side EffectsReports
B-cell Lymphoma Stage Iv 1
Hallucination 1
Paranoia 1

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Listril reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
    FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

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    Listril Safety Alerts, Active Ingredients, Usage Information

    More About Listril

    Side Effects reported to FDA: 3

    Listril safety alerts: No

    Reported hospitalizations: 1

    Latest Listril clinical trials