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Dolonex Side Effects

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Common Dolonex Side Effects


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

Genital Discomfort (2)
Vomiting (2)
Tetany (2)
Loss Of Consciousness (2)
Duodenal Ulcer (1)
Circulatory Collapse (1)
Urinary Retention (1)
Face Oedema (1)
Blood Pressure Abnormal (1)
Chest Discomfort (1)
Pulse Pressure Decreased (1)
Nausea (1)
Melaena (1)
Oedema Peripheral (1)
Pallor (1)
Hypotension (1)
Haemoglobin Decreased (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.

Dolonex Side Effects Reported to FDA



Dolonex Side Effect Report#7364665-7
Urinary Retention
This is a report of a 44-year-old female patient (weight: NA) from India, suffering from the following health symptoms/conditions: pain, who was treated with Dolonex (dosage: 2 Ml, 1x/day, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Urinary Retention after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Dolonex treatment in female patients, resulting in Urinary Retention side effect.
Dolonex Side Effect Report#5509484-9
Genital Discomfort
This report suggests a potential Dolonex Dt Genital Discomfort side effect(s) that can have serious consequences. A 27-year-old male patient (weight: NA) from India was diagnosed with the following symptoms/conditions: pain and used Dolonex Dt (dosage: NA) starting NS. After starting Dolonex Dt the patient began experiencing various side effects, including: Genital DiscomfortAdditional drugs used concurrently: NA. Although Dolonex Dt demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Genital Discomfort, may still occur.
Dolonex Side Effect Report#5499930-1
Genital Discomfort
This Genital Discomfort problem was reported by a physician from India. A 27-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: pain. On NS this consumer started treatment with Dolonex Dt (dosage: NA). The following drugs were being taken at the same time: NA. When using Dolonex Dt, the patient experienced the following unwanted symptoms/side effects: Genital DiscomfortAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Genital Discomfort, may become evident only after a product is in use by the general population.
Dolonex Side Effect Report#5322814-6
Chest Discomfort, Circulatory Collapse, Duodenal Ulcer, Haemoglobin Decreased, Hypotension, Melaena, Nausea, Pallor, Pulse Pressure Decreased
This Chest Discomfort side effect was reported by a physician from India. A 64-year-old male patient (weight:NA) experienced the following symptoms/conditions: arthralgia,arthritis.The patient was prescribed Dolonex Dt (drug dosage: NA), which was initiated on
Jan 24, 2007. Concurrently used drugs: NA..After starting to take Dolonex Dt the consumer reported adverse symptoms, such as: Chest Discomfort, Circulatory Collapse, Duodenal Ulcer, Haemoglobin Decreased, Hypotension, Melaena, Nausea, Pallor, Pulse Pressure DecreasedThese side effects may potentially be related to Dolonex Dt. The patient was hospitalized.
Dolonex Side Effect Report#5264135-6
Loss Of Consciousness, Tetany, Vomiting
This is a report of a 25-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: pain, who was treated with Dolonex (dosage: NA, start time:
Feb 23, 2007), combined with: NA. and developed a serious reaction and side effect(s): Loss Of Consciousness, Tetany, Vomiting after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Dolonex treatment in male patients, resulting in Loss Of Consciousness side effect. The patient was hospitalized.
Dolonex Side Effect Report#5258123-3
Loss Of Consciousness, Tetany, Vomiting
This report suggests a potential Dolonex Loss Of Consciousness side effect(s) that can have serious consequences. A 25-year-old male patient (weight: NA) from India was diagnosed with the following symptoms/conditions: pain and used Dolonex (dosage: NA) starting
Feb 23, 2007. After starting Dolonex the patient began experiencing various side effects, including: Loss Of Consciousness, Tetany, VomitingAdditional drugs used concurrently: NA.The patient was hospitalized. Although Dolonex demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Loss Of Consciousness, may still occur.
Dolonex Side Effect Report#5198153-3
Face Oedema, Oedema Peripheral
This Face Oedema problem was reported by a physician from India. A 35-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: osteoarthritis. On NS this consumer started treatment with Dolonex Dt (piroxicam) (dosage: 20 Mg (20 Mg, 1 In 1 D), Oral). The following drugs were being taken at the same time:
  • Cimetidine
When using Dolonex Dt (piroxicam), the patient experienced the following unwanted symptoms/side effects: Face Oedema, Oedema PeripheralAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Face Oedema, may become evident only after a product is in use by the general population.
Dolonex Side Effect Report#4951549-4
Blood Pressure Abnormal
This Blood Pressure Abnormal side effect was reported by a pharmacist from India. A 28-year-old male patient (weight:NA) experienced the following symptoms/conditions: pain.The patient was prescribed Dolonex Dt (piroxicam (drug dosage: 20 Mg (20 Mg, Single Dose), Oral), which was initiated on
Mar 08, 2006. Concurrently used drugs: NA..After starting to take Dolonex Dt (piroxicam the consumer reported adverse symptoms, such as: Blood Pressure AbnormalThese side effects may potentially be related to Dolonex Dt (piroxicam. The patient was hospitalized.



The appearance of Dolonex 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 Dolonex Side Effects for Women?

Women Side EffectsReports
Face Oedema 1
Oedema Peripheral 1
Urinary Retention 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.

    Dolonex 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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