Common Omesar Side Effects


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

Thrombocytopenia (2)
Increased Tendency To Bruise (2)
Lymphoma (1)
Osteoarthritis (1)
Hypotension (1)
Neutropenia (1)
Circulatory Collapse (1)
Arthralgia (1)
Biopsy Bone Marrow Abnormal (1)
Condition Aggravated (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.

Omesar Side Effects Reported to FDA



Omesar Side Effect Report#9773705
Hypotension, Circulatory Collapse
This is a report of a 61-year-old male patient (weight: NA) from IE, suffering from the following health symptoms/conditions: hypertension, who was treated with Omesar (dosage: NA, start time:
Aug 02, 2011), combined with:
  • Ulcid
  • Tenoret (chlortalidone, Atenolol) (50 Milligram) (chlortalidone, Atenolol)
  • Aspirin (accetylsalicylic Acid) (75 Milligram) (acetylsalicylic Acid)
  • Diovan (valsartan (40 Milligram) (valsartan)
and developed a serious reaction and side effect(s): Hypotension, Circulatory Collapse after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Omesar treatment in male patients, resulting in Hypotension side effect. The patient was hospitalized.
Omesar Side Effect Report#6796344-9
Neutropenia
This report suggests a potential Omesar (olmesartan Medoxomil) (tablet) (olmesartan Medoxomil) Neutropenia side effect(s) that can have serious consequences. A 52-year-old male patient (weight: NA) from Ireland was diagnosed with the following symptoms/conditions: hypertension and used Omesar (olmesartan Medoxomil) (tablet) (olmesartan Medoxomil) (dosage: 20 Mg, Oral; 40 Mg, Oral) starting
Jan 15, 2010. After starting Omesar (olmesartan Medoxomil) (tablet) (olmesartan Medoxomil) the patient began experiencing various side effects, including: NeutropeniaAdditional drugs used concurrently: NA. Although Omesar (olmesartan Medoxomil) (tablet) (olmesartan Medoxomil) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Neutropenia, may still occur.
Omesar Side Effect Report#6416623-4
Biopsy Bone Marrow Abnormal, Increased Tendency To Bruise, Lymphoma, Thrombocytopenia
This Biopsy Bone Marrow Abnormal problem was reported by a health professional from Italy. A 56-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On
Jan 01, 2008 this consumer started treatment with Omesar (olmesartan Medoxomil) (20 Milligram) (olmesartan Medoxomil) (dosage: Oral). The following drugs were being taken at the same time: NA. When using Omesar (olmesartan Medoxomil) (20 Milligram) (olmesartan Medoxomil), the patient experienced the following unwanted symptoms/side effects: Biopsy Bone Marrow Abnormal, Increased Tendency To Bruise, Lymphoma, ThrombocytopeniaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Biopsy Bone Marrow Abnormal, may become evident only after a product is in use by the general population.
Omesar Side Effect Report#6335833-8
Increased Tendency To Bruise, Thrombocytopenia
This Increased Tendency To Bruise side effect was reported by a consumer or non-health professional from Ireland. A 56-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Omesar (olmesartan Medoxomil) (20 Milligram) (olmesartan Medoxomil) (drug dosage: Oral), which was initiated on
Jan 01, 2008. Concurrently used drugs: NA..After starting to take Omesar (olmesartan Medoxomil) (20 Milligram) (olmesartan Medoxomil) the consumer reported adverse symptoms, such as: Increased Tendency To Bruise, ThrombocytopeniaThese side effects may potentially be related to Omesar (olmesartan Medoxomil) (20 Milligram) (olmesartan Medoxomil).
Omesar Side Effect Report#5331077-7
Arthralgia, Condition Aggravated, Osteoarthritis
This is a report of a 55-year-old male patient (weight: NA) from Ireland, suffering from the following health symptoms/conditions: hypertension, who was treated with Omesar (olmesartan Medoxomil) (20 Milligram, Tablet) (olmesartan Medox (dosage: 20 Mg (20 Mg, 1 In 1 D), Oral, start time:
Feb 01, 2007), combined with: NA. and developed a serious reaction and side effect(s): Arthralgia, Condition Aggravated, Osteoarthritis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Omesar (olmesartan Medoxomil) (20 Milligram, Tablet) (olmesartan Medox treatment in male patients, resulting in Arthralgia side effect.



The appearance of Omesar 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 Omesar Side Effects for Women?

Women Side Effects Reports
Increased Tendency To Bruise 2
Thrombocytopenia 2
Biopsy Bone Marrow Abnormal 1
Lymphoma 1

What are common Omesar Side Effects for Men?

Men Side Effects Reports
Arthralgia 1
Circulatory Collapse 1
Condition Aggravated 1
Hypotension 1
Neutropenia 1
Osteoarthritis 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.

    Omesar 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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    Omesar Safety Alerts, Active Ingredients, Usage Information

    More About Omesar

    Side Effects reported to FDA: 5

    Omesar safety alerts: No

    Reported hospitalizations: 1

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