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Voveran Side Effects

PatientsVille

Common Voveran Side Effects


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

Asthenia (5)
Rash (4)
Pruritus (4)
Hypoaesthesia (4)
Abasia (4)
Corneal Epithelium Defect (4)
Erythema (3)
Dizziness (3)
Injection Site Erythema (3)
Injection Site Induration (3)
Dyspnoea (2)
Corneal Perforation (2)
Hypotension (2)
Injection Site Swelling (2)
Paraesthesia (2)
Ocular Hyperaemia (2)
Lacrimation Increased (1)
Macroglossia (1)
Nausea (1)
Multi-organ Failure (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.

Voveran Side Effects Reported to FDA



Voveran Side Effect Report#6609769-9
Conjunctival Hyperaemia, Corneal Oedema, Corneal Perforation, Corneal Thinning, Eye Pain, Lacrimation Increased, Ocular Hyperaemia
This is a report of a 19-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: NA, who was treated with Voveran Ophthalmic (nvo) (dosage: 0.1 %, 5 Times In A Day, start time: NS), combined with:
  • Dexamethasone
  • Proparacaine Hcl (Unk)
  • Ofloxacin
  • Riboflavin Tab
  • Antiinfl. Prep., Non-steroids For Topical Use
  • Carboxymethylcellulose Sodium (4 Times A Day In Both Eyes)
and developed a serious reaction and side effect(s): Conjunctival Hyperaemia, Corneal Oedema, Corneal Perforation, Corneal Thinning, Eye Pain, Lacrimation Increased, Ocular Hyperaemia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Voveran Ophthalmic (nvo) treatment in male patients, resulting in Conjunctival Hyperaemia side effect.
Voveran Side Effect Report#5405689-6
Injection Site Erythema, Injection Site Induration
This report suggests a potential Voveran Injection Site Erythema side effect(s) that can have serious consequences. A 30-year-old female patient (weight: NA) from India was diagnosed with the following symptoms/conditions: pain and used Voveran (dosage: NA) starting NS. After starting Voveran the patient began experiencing various side effects, including: Injection Site Erythema, Injection Site IndurationAdditional drugs used concurrently:
  • Hydroxychloroquine Sulfate
  • Mexate
Although Voveran demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Injection Site Erythema, may still occur.
Voveran Side Effect Report#5405682-3
Injection Site Erythema, Injection Site Induration
This Injection Site Erythema problem was reported by a physician from India. A 53-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Voveran (dosage: NA). The following drugs were being taken at the same time:
  • Tramadol Hcl
  • Cefuroxime
  • Gentamicin
When using Voveran, the patient experienced the following unwanted symptoms/side effects: Injection Site Erythema, Injection Site IndurationAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Injection Site Erythema, may become evident only after a product is in use by the general population.
Voveran Side Effect Report#5405617-3
Injection Site Erythema, Injection Site Induration
This Injection Site Erythema side effect was reported by a physician from India. A 22-year-old female patient (weight:NA) experienced the following symptoms/conditions: pain.The patient was prescribed Voveran (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Cefuroxime
  • Gentamicin
.After starting to take Voveran the consumer reported adverse symptoms, such as: Injection Site Erythema, Injection Site IndurationThese side effects may potentially be related to Voveran.
Voveran Side Effect Report#5398894-9
Cough, Dyspnoea, Macroglossia, Palpitations, Pruritus, Rash
This is a report of a 63-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: back pain, who was treated with Voveran (dosage: 50 Mg, Qd, start time:
Jul 21, 2007), combined with: NA. and developed a serious reaction and side effect(s): Cough, Dyspnoea, Macroglossia, Palpitations, Pruritus, Rash after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Voveran treatment in male patients, resulting in Cough side effect.
Voveran Side Effect Report#5303137-8
Blood Pressure Decreased, Eye Pruritus, Feeling Abnormal, Ocular Hyperaemia, Pulse Abnormal, Restlessness
This report suggests a potential Voveran Plus Blood Pressure Decreased side effect(s) that can have serious consequences. A 62-year-old female patient (weight: NA) from India was diagnosed with the following symptoms/conditions: NA and used Voveran Plus (dosage: Diclo 50 / Para 500 Mg/day) starting NS. After starting Voveran Plus the patient began experiencing various side effects, including: Blood Pressure Decreased, Eye Pruritus, Feeling Abnormal, Ocular Hyperaemia, Pulse Abnormal, RestlessnessAdditional drugs used concurrently:
  • Paracetamol (1 Ml/day)
Although Voveran Plus demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Blood Pressure Decreased, may still occur.
Voveran Side Effect Report#5157214-5
Radial Nerve Palsy
This Radial Nerve Palsy problem was reported by a consumer or non-health professional from India. A 30-year-old patient (weight: NA) was diagnosed with the following symptoms/conditions: back pain. On NS this consumer started treatment with Voveran (dosage: 3 Ml, Unk). The following drugs were being taken at the same time: NA. When using Voveran, the patient experienced the following unwanted symptoms/side effects: Radial Nerve PalsyAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Radial Nerve Palsy, may become evident only after a product is in use by the general population.
Voveran Side Effect Report#5153082-6
Haemoglobin Decreased, Otorrhoea, Tympanic Membrane Perforation
This Haemoglobin Decreased side effect was reported by a physician from India. A 56-year-old male patient (weight:NA) experienced the following symptoms/conditions: musculoskeletal pain.The patient was prescribed Voveran (drug dosage: 100 Mg/day), which was initiated on
Aug 01, 2006. Concurrently used drugs:
  • Lopril
  • Wysolone (5 Mg, Unk)
  • Xantinol Nicotinate
.After starting to take Voveran the consumer reported adverse symptoms, such as: Haemoglobin Decreased, Otorrhoea, Tympanic Membrane PerforationThese side effects may potentially be related to Voveran.
Voveran Side Effect Report#5125015-X
Circulatory Collapse, Dizziness, Dyspnoea, Pruritus
This is a report of a 72-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: arthralgia, who was treated with Voveran (dosage: 3 Ml, Once/single, start time: NS), combined with:
  • Gentamicin (2 Ml, Unk)
and developed a serious reaction and side effect(s): Circulatory Collapse, Dizziness, Dyspnoea, Pruritus after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Voveran treatment in male patients, resulting in Circulatory Collapse side effect.
Voveran Side Effect Report#5044309-X
Abdominal Pain Upper, Ileus Paralytic
This report suggests a potential Voveran Abdominal Pain Upper side effect(s) that can have serious consequences. A 22-year-old female patient (weight: NA) from India was diagnosed with the following symptoms/conditions: procedural pain and used Voveran (dosage: Two Injection At A Gap Of 15 Hours) starting NS. After starting Voveran the patient began experiencing various side effects, including: Abdominal Pain Upper, Ileus ParalyticAdditional drugs used concurrently:
  • Ranitidine
  • Pantoprazole
  • Ketamine Hcl
The patient was hospitalized. Although Voveran demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Abdominal Pain Upper, may still occur.
Voveran Side Effect Report#5042453-4
Asthenia, Dizziness, Erythema, Feeling Cold, Flushing, Hypotension, Nausea, Pruritus, Vertigo
This Asthenia problem was reported by a physician from India. A 60-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: pain. On NS this consumer started treatment with Voveran (dosage: NA). The following drugs were being taken at the same time:
  • Avil
  • Dexona
  • Adrenaline (0.5 Ml, Unk)
When using Voveran, the patient experienced the following unwanted symptoms/side effects: Asthenia, Dizziness, Erythema, Feeling Cold, Flushing, Hypotension, Nausea, Pruritus, VertigoThe 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 Asthenia, may become evident only after a product is in use by the general population.
Voveran Side Effect Report#4987043-4
Erythema, Injection Site Swelling, Rash
This Erythema side effect was reported by a physician from India. A 55-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Voveran (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Monocef
  • Amikacin
  • Fenergan
.After starting to take Voveran the consumer reported adverse symptoms, such as: Erythema, Injection Site Swelling, RashThese side effects may potentially be related to Voveran.
Voveran Side Effect Report#4971476-6
Erythema, Injection Site Swelling, Rash
This is a report of a 55-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: NA, who was treated with Voveran (dosage: NA, start time: NS), combined with:
  • Monocef
  • Amikacin
  • Fenergan
and developed a serious reaction and side effect(s): Erythema, Injection Site Swelling, Rash after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Voveran treatment in male patients, resulting in Erythema side effect.
Voveran Side Effect Report#4714451-9
Corneal Epithelium Defect
This report suggests a potential Voveran Ophthalmic (nvo) Corneal Epithelium Defect side effect(s) that can have serious consequences. A 58-year-old male patient (weight: NA) from India was diagnosed with the following symptoms/conditions: inflammation,prophylaxis and used Voveran Ophthalmic (nvo) (dosage: Unk, Qid) starting NS. After starting Voveran Ophthalmic (nvo) the patient began experiencing various side effects, including: Corneal Epithelium DefectAdditional drugs used concurrently: NA. Although Voveran Ophthalmic (nvo) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Corneal Epithelium Defect, may still occur.
Voveran Side Effect Report#4714446-5
Corneal Epithelium Defect
This Corneal Epithelium Defect problem was reported by a physician from India. A 28-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Voveran Ophthalmic (nvo) (dosage: Unk, Qid). The following drugs were being taken at the same time:
  • Prednisolone Acetate
  • Timolet P
When using Voveran Ophthalmic (nvo), the patient experienced the following unwanted symptoms/side effects: Corneal Epithelium DefectAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Corneal Epithelium Defect, may become evident only after a product is in use by the general population.
Voveran Side Effect Report#4714445-3
Corneal Perforation, Ulcerative Keratitis
This Corneal Perforation side effect was reported by a physician from India. A 80-year-old female patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Voveran Ophthalmic (nvo) (drug dosage: Unk, Qid), which was initiated on NS. Concurrently used drugs:
  • Prednisolone Acetate
  • Antiglaucoma Preparations And Miotics
.After starting to take Voveran Ophthalmic (nvo) the consumer reported adverse symptoms, such as: Corneal Perforation, Ulcerative KeratitisThese side effects may potentially be related to Voveran Ophthalmic (nvo).
Voveran Side Effect Report#4714444-1
Corneal Epithelium Defect
This is a report of a 58-year-old male patient (weight: NA) from India, suffering from the following health symptoms/conditions: post procedural complication, who was treated with Voveran Ophthalmic (nvo) (dosage: Unk, Qid, start time: NS), combined with:
  • Prednisolone Acetate
and developed a serious reaction and side effect(s): Corneal Epithelium Defect after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Voveran Ophthalmic (nvo) treatment in male patients, resulting in Corneal Epithelium Defect side effect.
Voveran Side Effect Report#4714442-8
Corneal Epithelium Defect
This report suggests a potential Voveran Ophthalmic (nvo) Corneal Epithelium Defect side effect(s) that can have serious consequences. A 70-year-old male patient (weight: NA) from India was diagnosed with the following symptoms/conditions: NA and used Voveran Ophthalmic (nvo) (dosage: Unk, Qid) starting NS. After starting Voveran Ophthalmic (nvo) the patient began experiencing various side effects, including: Corneal Epithelium DefectAdditional drugs used concurrently:
  • Prednisolone Acetate
Although Voveran Ophthalmic (nvo) demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Corneal Epithelium Defect, may still occur.
Voveran Side Effect Report#4669915-3
Gastrointestinal Haemorrhage, Haematemesis
This Gastrointestinal Haemorrhage problem was reported by a physician from . A 76-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: femur fracture. On NS this consumer started treatment with Voveran (dosage: 50 Mg, Bid). The following drugs were being taken at the same time:
  • Taxim (1 G, Bid)
  • Gentamicin (80 Mg, Bid)
  • Rantac (150 Mg, Qd)
  • Carbamazepine (100 Mg/day)
When using Voveran, the patient experienced the following unwanted symptoms/side effects: Gastrointestinal Haemorrhage, HaematemesisThe 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 Gastrointestinal Haemorrhage, may become evident only after a product is in use by the general population.
Voveran Side Effect Report#4644689-0
Dizziness, Ecg Signs Of Myocardial Ischaemia, Hypotension, Pruritus, Pulse Absent, Rash
This Dizziness side effect was reported by a physician from . A 70-year-old female patient (weight:NA) experienced the following symptoms/conditions: periarthritis.The patient was prescribed Voveran (drug dosage: 75 Mg, Once/single), which was initiated on NS. Concurrently used drugs: NA..After starting to take Voveran the consumer reported adverse symptoms, such as: Dizziness, Ecg Signs Of Myocardial Ischaemia, Hypotension, Pruritus, Pulse Absent, RashThese side effects may potentially be related to Voveran. The patient was hospitalized.
Voveran Side Effect Report#4556074-0
Abasia, Asthenia, Gait Disturbance, Hypoaesthesia
This is a report of a 34-year-old male patient (weight: NA) from , suffering from the following health symptoms/conditions: pain, who was treated with Voveran (dosage: 75 Mg, Once/single, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Abasia, Asthenia, Gait Disturbance, Hypoaesthesia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Voveran treatment in male patients, resulting in Abasia side effect.
Voveran Side Effect Report#4556073-9
Abasia, Asthenia, Hypoaesthesia, Paraesthesia
This report suggests a potential Voveran Abasia side effect(s) that can have serious consequences. A 48-year-old male patient (weight: NA) from was diagnosed with the following symptoms/conditions: back pain and used Voveran (dosage: 75 Mg, Once/single) starting NS. After starting Voveran the patient began experiencing various side effects, including: Abasia, Asthenia, Hypoaesthesia, ParaesthesiaAdditional drugs used concurrently: NA. Although Voveran demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Abasia, may still occur.
Voveran Side Effect Report#4546308-0
Abasia, Asthenia, Hypoaesthesia
This Abasia problem was reported by a physician from . A 34-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: pain. On NS this consumer started treatment with Voveran (dosage: 75 Mg, Once/single). The following drugs were being taken at the same time: NA. When using Voveran, the patient experienced the following unwanted symptoms/side effects: Abasia, Asthenia, HypoaesthesiaAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Abasia, may become evident only after a product is in use by the general population.
Voveran Side Effect Report#4546306-7
Abasia, Asthenia, Hypoaesthesia, Paraesthesia
This Abasia side effect was reported by a physician from . A 48-year-old male patient (weight:NA) experienced the following symptoms/conditions: back pain.The patient was prescribed Voveran (drug dosage: 75 Mg, Once/single), which was initiated on NS. Concurrently used drugs: NA..After starting to take Voveran the consumer reported adverse symptoms, such as: Abasia, Asthenia, Hypoaesthesia, ParaesthesiaThese side effects may potentially be related to Voveran.
Voveran Side Effect Report#10003609
Acute Respiratory Distress Syndrome, Multi-organ Failure
This is a report of a 23-year-old male patient (weight: NA) from IN, suffering from the following health symptoms/conditions: pyrexia,pain, who was treated with Voveran (dosage: 75 Mg, Unk, start time: NS), combined with: NA. and developed a serious reaction and side effect(s): Acute Respiratory Distress Syndrome, Multi-organ Failure after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Voveran treatment in male patients, resulting in Acute Respiratory Distress Syndrome side effect.



The appearance of Voveran 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.


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.

    Voveran 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 Voveran

    Side Effects reported to FDA: 25

    Voveran safety alerts: No

    Reported deaths: 2

    Reported hospitalizations: 5

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