Secotex Ocas Side Effects


Common Secotex Ocas Side Effects

The most commonly reported Secotex Ocas side effects are:
No Ejaculation (14)
Ejaculation (10)
Dry Mouth (4)
Extreme Dizziness...take At Night Only (1)

If you have experienced a side effect listed above, you can check a box to report it.

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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.

Secotex Ocas Side Effects Reported to FDA

Secotex Ocas Side Effect Report#6602223-X
This is a report of a 56-year-old male patient (weight: NA) from , suffering from the following health symptoms/conditions: benign prostatic hyperplasia, who was treated with Secotex Ocas (dosage: One Tablet Every Day, start time:
Feb 17, 2010), combined with: NA. and developed a serious reaction and side effect(s): Hypersensitivity after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Secotex Ocas treatment in male patients, resulting in Hypersensitivity side effect.
Secotex Ocas Side Effect Report#6132406-7
Dry Mouth, Headache, Hypotension, Nausea, Vertigo
This report suggests a potential Secotex Ocas Dry Mouth side effect(s) that can have serious consequences. A 62-year-old male patient (weight: NA) from was diagnosed with the following symptoms/conditions: benign prostatic hyperplasia,diabetes mellitus,hypertension and used Secotex Ocas (dosage: .4mg) starting
Mar 19, 2009. After starting Secotex Ocas the patient began experiencing various side effects, including: Dry Mouth, Headache, Hypotension, Nausea, VertigoAdditional drugs used concurrently:
  • Insulin
  • Aspirin
  • Atacand
Although Secotex Ocas demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Dry Mouth, may still occur.

The appearance of Secotex Ocas 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 Secotex Ocas Side Effects for Women?

Women Side EffectsReports

What are common Secotex Ocas Side Effects for Men?

Men Side EffectsReports
Dry Mouth 1
Headache 1
Hypersensitivity 1
Hypotension 1
Nausea 1
Vertigo 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.

    Secotex Ocas 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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    Secotex Ocas Safety Alerts, Active Ingredients, Usage Information

    More About Secotex ocas

    Side Effects reported to FDA: 2

    Secotex Ocas safety alerts: No

    Latest Secotex Ocas clinical trials