Common Konverge Side Effects

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

Hypersensitivity (2)
Oedema Peripheral (1)
Hyponatraemia (1)
Dizziness (1)
Anaemia (1)
Erectile Dysfunction (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.

Konverge Side Effects Reported to FDA

Konverge Side Effect Report#9678400
This is a report of a 64-year-old male patient (weight: NA) from IE, suffering from the following health symptoms/conditions: hypertension, who was treated with Konverge (dosage: NA, start time:
Jan 21, 2013), combined with:
  • Nuseal Aspirin (aetylsalicylic Acid) (aceytlsalicylic Acid)
  • Esomeprazole (esomeprazole) (esomeprazole)
  • Nebivolol (nebivolol) (nebivolol)
and developed a serious reaction and side effect(s): Hyponatraemia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Konverge treatment in male patients, resulting in Hyponatraemia side effect. The patient was hospitalized.
Konverge Side Effect Report#8204834-7
Erectile Dysfunction, Dizziness
This report suggests a potential Konverge (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesar Erectile Dysfunction side effect(s) that can have serious consequences. A 41-year-old male patient (weight: NA) from Italy was diagnosed with the following symptoms/conditions: hypertension and used Konverge (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesar (dosage: 40/10 Mg, Oral) starting
Jan 03, 2012. After starting Konverge (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesar the patient began experiencing various side effects, including: Erectile Dysfunction, DizzinessAdditional drugs used concurrently: NA. Although Konverge (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesar demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Erectile Dysfunction, may still occur.
Konverge Side Effect Report#7889046-9
This Anaemia problem was reported by a health professional from Ireland. A 64-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Konverge (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesar (dosage: 20/5 Mg, Oral). The following drugs were being taken at the same time: NA. When using Konverge (olmesartan Medoxomil, Amlodipine Besilate) (tablet) (olmesar, the patient experienced the following unwanted symptoms/side effects: AnaemiaThe 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 Anaemia, may become evident only after a product is in use by the general population.
Konverge Side Effect Report#6579076-1
This Hypersensitivity side effect was reported by a physician from Italy. A 78-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Konverge (olmesartan Medoxomil/amlodipine Besilate) (tablet) (drug dosage: 40/10 Mg (1 In 1 D), Oral), which was initiated on
Nov 01, 2009. Concurrently used drugs:
  • Pravitin (pravastatin Sodium) (10 Milligram) (pravastatin Sodium)
  • Xalatan (latanoprost) (eye Drops) (latanoprost)
  • Aspirin Nuseal (acetylsalicylic Acid) (75 Milligram) (acetylsalicylic
  • Co-diovan (hydrochlorothiazide, Valsartan) (hydrochlorothiazide, Valsa
  • Zanedip (lercanidipine Hydrochloride) (lercanidipine Hydrochloride)
.After starting to take Konverge (olmesartan Medoxomil/amlodipine Besilate) (tablet) the consumer reported adverse symptoms, such as: HypersensitivityThese side effects may potentially be related to Konverge (olmesartan Medoxomil/amlodipine Besilate) (tablet).
Konverge Side Effect Report#6573955-7
Hypersensitivity, Oedema Peripheral
This is a report of a 85-year-old female patient (weight: NA) from Ireland, suffering from the following health symptoms/conditions: hypertension, who was treated with Konverge (olmesartan Medoxomil/amlodipine Besilate Tablet) (dosage: Oral, start time:
Dec 01, 2009), combined with:
  • Allopurinol
  • Doxazosin (doxazosin) (doxazosin)
  • Rasilez (aliskiren)
  • Nebilet (nebivolol Hydrochloride) (nebivolol Hydrochloride)
and developed a serious reaction and side effect(s): Hypersensitivity, Oedema Peripheral after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Konverge (olmesartan Medoxomil/amlodipine Besilate Tablet) treatment in female patients, resulting in Hypersensitivity side effect.

The appearance of Konverge 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 Konverge Side Effects for Women?

Women Side Effects Reports
Hypersensitivity 2
Anaemia 1
Oedema Peripheral 1

What are common Konverge Side Effects for Men?

Men Side Effects Reports
Dizziness 1
Erectile Dysfunction 1
Hyponatraemia 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.

    Konverge 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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    Konverge Safety Alerts, Active Ingredients, Usage Information

    More About Konverge

    Side Effects reported to FDA: 5

    Konverge safety alerts: No

    Reported hospitalizations: 1

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