Common Zolnor Side Effects

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

Blood Creatinine Increased (1)
Blood Bilirubin Increased (1)
Blister (1)
Pruritus (1)
Dizziness (1)
Ecchymosis (1)
Neoplasm Malignant (1)
Hepatocellular Carcinoma (1)
Erectile Dysfunction (1)
Alpha 1 Foetoprotein Increased (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.

Zolnor Side Effects Reported to FDA

Zolnor Side Effect Report#9424746
Hepatocellular Carcinoma, Alpha 1 Foetoprotein Increased, Blood Bilirubin Increased, Blood Creatinine Increased, Neoplasm Malignant
This is a report of a 62-year-old male patient (weight: NA) from IT, suffering from the following health symptoms/conditions: NA, who was treated with Zolnor (dosage: NA, start time: 201206), combined with:
  • Acetylsalicylic Acid
  • Simvastatine (simvastatin)
  • Spironolactone
and developed a serious reaction and side effect(s): Hepatocellular Carcinoma, Alpha 1 Foetoprotein Increased, Blood Bilirubin Increased, Blood Creatinine Increased, Neoplasm Malignant after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Zolnor treatment in male patients, resulting in Hepatocellular Carcinoma side effect.
Zolnor Side Effect Report#8255599-4
This report suggests a potential Zolnor (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (omesartan Ecchymosis side effect(s) that can have serious consequences. A 56-year-old female patient (weight: NA) from Portugal was diagnosed with the following symptoms/conditions: NA and used Zolnor (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (omesartan (dosage: 20/5 Mg,oral) starting
Feb 09, 2012. After starting Zolnor (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (omesartan the patient began experiencing various side effects, including: EcchymosisAdditional drugs used concurrently: NA. Although Zolnor (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (omesartan demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Ecchymosis, may still occur.
Zolnor Side Effect Report#7166428-4
Blister, Dizziness, Pruritus
This Blister problem was reported by a consumer or non-health professional from Italy. A 54-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On
Nov 04, 2010 this consumer started treatment with Zolnor (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesarta (dosage: 20/5 Mg, Oral). The following drugs were being taken at the same time:
  • Nebilet (nebivolol Hydrochloride) (nebivolol Hydrochloride)
When using Zolnor (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesarta, the patient experienced the following unwanted symptoms/side effects: Blister, Dizziness, PruritusAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Blister, may become evident only after a product is in use by the general population.
Zolnor Side Effect Report#7138024-6
Erectile Dysfunction
This Erectile Dysfunction side effect was reported by a consumer or non-health professional from Italy. A 56-year-old male patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Zolnor (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesarta (drug dosage: Oral), which was initiated on
Oct 20, 2010. Concurrently used drugs: NA..After starting to take Zolnor (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesarta the consumer reported adverse symptoms, such as: Erectile DysfunctionThese side effects may potentially be related to Zolnor (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesarta.

The appearance of Zolnor 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 Zolnor Side Effects for Women?

Women Side Effects Reports
Blister 1
Dizziness 1
Ecchymosis 1
Pruritus 1

What are common Zolnor Side Effects for Men?

Men Side Effects Reports
Alpha 1 Foetoprotein Increased 1
Blood Bilirubin Increased 1
Blood Creatinine Increased 1
Erectile Dysfunction 1
Hepatocellular Carcinoma 1
Neoplasm Malignant 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.

    Zolnor 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.

    Discuss Zolnor Side Effects

    Did You Have a Zolnor Side Effect?

    Yes, Severe
    Yes, Moderate
    Yes, Minor

    How Effective is Zolnor for You?

    Exceeded Expectations
    Somewhat Effective
    Not Effective

    Zolnor Safety Alerts, Active Ingredients, Usage Information

    More About Zolnor

    Side Effects reported to FDA: 4

    Zolnor safety alerts: No

    Reported deaths: 1

    Latest Zolnor clinical trials

    Zolnor Reviews

    No reviews, be a first to report a side effect via side effect reporting form

    Popular Pages