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Neogynon Side Effects

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Common Neogynon Side Effects


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

Cerebral Infarction (2)
Prothrombin Time Shortened (2)
Dyspnoea (2)
Genital Haemorrhage (2)
Coagulation Factor V Level Decreased (2)
Cerebral Thrombosis (2)
Blood Pressure Systolic Decreased (1)
Dehydration (1)
Blood Pressure Systolic Increased (1)
Vertigo (1)
Dry Eye (1)
Asthenia (1)
Blood Pressure Diastolic Increased (1)
Personality Disorder (1)
Mood Altered (1)
Influenza Like Illness (1)
Nausea (1)
Serotonin Syndrome (1)
Incontinence (1)
Haemoglobin Decreased (1)

➢ More



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.

Neogynon Side Effects Reported to FDA


Neogynon Side Effect Report#5476101-6
Asthenia, Dehydration, Dry Eye, Incontinence, Influenza Like Illness, Mood Altered, Nausea, Personality Disorder, Serotonin Syndrome
This is a report of a 34-year-old female patient (weight: NA) from Denmark, suffering from the following health symptoms/conditions: NA, who was treated with Neogynon (dosage: NA, start time:
Jan 01, 2007), combined with:
  • Cymbalta
and developed a serious reaction and side effect(s): Asthenia, Dehydration, Dry Eye, Incontinence, Influenza Like Illness, Mood Altered, Nausea, Personality Disorder, Serotonin Syndrome after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Neogynon treatment in female patients, resulting in Asthenia side effect.
Neogynon Side Effect Report#5109797-9
Blood Pressure Systolic Increased, Cerebral Infarction, Cerebral Thrombosis, Coagulation Factor V Level Decreased, Dyspnoea, Genital Haemorrhage, Haemoglobin Decreased, Prothrombin Time Shortened, Vertigo
This report suggests a potential Neogynon (levonorgestrel/ethinyl Estradiol, Tablet) Blood Pressure Systolic Increased side effect(s) that can have serious consequences. A 48-year-old female patient (weight: NA) from Denmark was diagnosed with the following symptoms/conditions: menorrhagia and used Neogynon (levonorgestrel/ethinyl Estradiol, Tablet) (dosage: See Image) starting
Jan 30, 2004. After starting Neogynon (levonorgestrel/ethinyl Estradiol, Tablet) the patient began experiencing various side effects, including: Blood Pressure Systolic Increased, Cerebral Infarction, Cerebral Thrombosis, Coagulation Factor V Level Decreased, Dyspnoea, Genital Haemorrhage, Haemoglobin Decreased, Prothrombin Time Shortened, VertigoAdditional drugs used concurrently: NA.The patient was hospitalized. Although Neogynon (levonorgestrel/ethinyl Estradiol, Tablet) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Pressure Systolic Increased, may still occur.
Neogynon Side Effect Report#5106846-9
Blood Pressure Diastolic Increased, Blood Pressure Systolic Decreased, Cerebral Infarction, Cerebral Thrombosis, Coagulation Factor V Level Decreased, Dyspnoea, Genital Haemorrhage, Prothrombin Time Shortened
This Blood Pressure Diastolic Increased problem was reported by a health professional from Denmark. A 48-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: menorrhagia. On
Jan 30, 2004 this consumer started treatment with Neogynon (levonorgestrel/ethinyl Estradiol, Tablet) (dosage: See Image). The following drugs were being taken at the same time: NA. When using Neogynon (levonorgestrel/ethinyl Estradiol, Tablet), the patient experienced the following unwanted symptoms/side effects: Blood Pressure Diastolic Increased, Blood Pressure Systolic Decreased, Cerebral Infarction, Cerebral Thrombosis, Coagulation Factor V Level Decreased, Dyspnoea, Genital Haemorrhage, Prothrombin Time ShortenedThe 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 Blood Pressure Diastolic Increased, may become evident only after a product is in use by the general population.



The appearance of Neogynon 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.

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What are common Neogynon Side Effects for Men?

Men Side EffectsReports

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.

    Neogynon 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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    More About Neogynon

    Side Effects reported to FDA: 3

    Neogynon safety alerts: No

    Reported hospitalizations: 3

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