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Karvea Side Effects

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Common Karvea Side Effects


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

Renal Failure Acute (7)
Hypotension (6)
Hyperkalaemia (6)
Hyponatraemia (5)
Dizziness (5)
Myalgia (4)
Suicide Attempt (4)
Bradycardia (4)
Tinnitus (4)
Overdose (4)
Angina Pectoris (3)
Blood Sodium Decreased (3)
Angioneurotic Oedema (3)
Atrial Fibrillation (3)
Mobility Decreased (3)
Hypertensive Crisis (3)
Nodal Arrhythmia (3)
Somnolence (3)
Syncope (3)
Pain In Extremity (3)

➢ 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.

Karvea Side Effects Reported to FDA



Karvea Side Effect Report#9840406
Pancreatitis Acute
This is a report of a 71-year-old male patient (weight: NA) from IT, suffering from the following health symptoms/conditions: hypertension, who was treated with Karvea (dosage: NA, start time:
Jan 01, 2013), combined with:
  • Metformin Hydrochloride
  • Lansoprazole
  • Torvast
  • Cardirene
  • Altiazem
and developed a serious reaction and side effect(s): Pancreatitis Acute after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Karvea treatment in male patients, resulting in Pancreatitis Acute side effect. The patient was hospitalized.
Karvea Side Effect Report#9781293
Syncope
This report suggests a potential Karvea Syncope side effect(s) that can have serious consequences. A 80-year-old female patient (weight: NA) from IT was diagnosed with the following symptoms/conditions: NA and used Karvea (dosage: NA) starting
Oct 07, 2012. After starting Karvea the patient began experiencing various side effects, including: SyncopeAdditional drugs used concurrently:
  • Lorazepam
  • Eutirox
Although Karvea demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Syncope, may still occur.
Karvea Side Effect Report#9628384
Psychomotor Retardation, Hypoglycaemia
This Psychomotor Retardation problem was reported by a physician from IT. A 80-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jan 01, 2013 this consumer started treatment with Karvea (dosage: Strength: 75 Mg). The following drugs were being taken at the same time:
  • Madopar
  • Torvast (Strength: 10 Mg)
  • Delecit (Strength: 400 Mg)
  • Exemestane (Strength: 25 Mg)
  • Lantus
  • Humalog
  • Pentoxifylline
When using Karvea, the patient experienced the following unwanted symptoms/side effects: Psychomotor Retardation, HypoglycaemiaThe 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 Psychomotor Retardation, may become evident only after a product is in use by the general population.
Karvea Side Effect Report#9411480
Blood Sodium Decreased, Syncope
This Blood Sodium Decreased side effect was reported by a consumer or non-health professional from DE. A 70-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Karvea (drug dosage: NA), which was initiated on NS. Concurrently used drugs:
  • Eferox (Eferox 50 (l-thyroxine).)
.After starting to take Karvea the consumer reported adverse symptoms, such as: Blood Sodium Decreased, SyncopeThese side effects may potentially be related to Karvea. The patient was hospitalized.
Karvea Side Effect Report#9168563
Palpitations, Dyspnoea, Cough, Flushing, Dysgeusia
This is a report of a 72-year-old female patient (weight: NA) from DE, suffering from the following health symptoms/conditions: hypertension, who was treated with Karvea (dosage: Central Pharmaceutical Number: 0647629, [v09/2014], 98 Tablets] 150 Mg 1-0-0, start time:
Jan 07, 2013), combined with: NA. and developed a serious reaction and side effect(s): Palpitations, Dyspnoea, Cough, Flushing, Dysgeusia after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Karvea treatment in female patients, resulting in Palpitations side effect.
Karvea Side Effect Report#9052561
Nodal Arrhythmia, Renal Failure Acute, Nodal Arrhythmia, Toxicity To Various Agents, Conduction Disorder, Bradycardia
This report suggests a potential Karvea Nodal Arrhythmia side effect(s) that can have serious consequences. A 72-year-old female patient (weight: NA) from IT was diagnosed with the following symptoms/conditions: hypertension,arrhythmia and used Karvea (dosage: NA) starting
Jun 01, 2012. After starting Karvea the patient began experiencing various side effects, including: Nodal Arrhythmia, Renal Failure Acute, Nodal Arrhythmia, Toxicity To Various Agents, Conduction Disorder, BradycardiaAdditional drugs used concurrently:
  • Lanoxin
  • Aldactone
  • Tareg
  • Lasix
  • Libradin
  • Congescor
  • Solosa
  • Nitroderm (Die Patches)
The patient was hospitalized. Although Karvea demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Nodal Arrhythmia, may still occur.
Karvea Side Effect Report#8962477
Dizziness, Tinnitus
This Dizziness problem was reported by a consumer or non-health professional from DE. A 64-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On 201204 this consumer started treatment with Karvea (dosage: NA). The following drugs were being taken at the same time: NA. When using Karvea, the patient experienced the following unwanted symptoms/side effects: Dizziness, TinnitusAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Dizziness, may become evident only after a product is in use by the general population.
Karvea Side Effect Report#8827537
Atrial Fibrillation, Hypokalaemia
This Atrial Fibrillation side effect was reported by a consumer or non-health professional from DE. A 63-year-old male patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Karvea (drug dosage: 1df:1/3 Of A Tab Daily), which was initiated on 201111. Concurrently used drugs:
  • Kalinor
  • Sotalex
.After starting to take Karvea the consumer reported adverse symptoms, such as: Atrial Fibrillation, HypokalaemiaThese side effects may potentially be related to Karvea.
Karvea Side Effect Report#8770191
Gastrointestinal Infection, Salpingo-oophoritis
This is a report of a 61-year-old female patient (weight: NA) from DE, suffering from the following health symptoms/conditions: hypertension,salpingo-oophoritis,arrhythmia,toxic nodular goitre, who was treated with Karvea (dosage: Jun2004-may2011: 150 Mg, Tabs, start time: 1989), combined with:
  • Azithromycin
  • Prajmalium Bitartrate (Tabs)
  • Levothyroxin (Tabs)
and developed a serious reaction and side effect(s): Gastrointestinal Infection, Salpingo-oophoritis after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Karvea treatment in female patients, resulting in Gastrointestinal Infection side effect.
Karvea Side Effect Report#8460172-9
Renal Cell Carcinoma, Ovarian Mass, Joint Swelling, Oedema Peripheral
This report suggests a potential Karvea Renal Cell Carcinoma side effect(s) that can have serious consequences. A female patient (weight: NA) from Australia was diagnosed with the following symptoms/conditions: NA and used Karvea (dosage: NA) starting NS. After starting Karvea the patient began experiencing various side effects, including: Renal Cell Carcinoma, Ovarian Mass, Joint Swelling, Oedema PeripheralAdditional drugs used concurrently:
  • Pradaxa (220 Mg)
  • Crestor
  • Lasix
  • Protos
Although Karvea demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Renal Cell Carcinoma, may still occur.
Karvea Side Effect Report#8399087-3
Acute Prerenal Failure, Nodal Arrhythmia
This Acute Prerenal Failure problem was reported by a health professional from Italy. A 85-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Jan 01, 2010 this consumer started treatment with Karvea (dosage: 300 Mg). The following drugs were being taken at the same time:
  • Adalat (60 Mg)
  • Atorvastatin Calcium (10 Mg)
  • Kilor (1 Sachet)
  • Omapren (20 Mg)
  • Novolog Mix 70/30 (64 Iu)
  • Furosemide (80 Mg)
  • Allopurinol (100 Mg)
  • Nebivolol (5 Mg)
When using Karvea, the patient experienced the following unwanted symptoms/side effects: Acute Prerenal Failure, Nodal ArrhythmiaThe 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 Acute Prerenal Failure, may become evident only after a product is in use by the general population.
Karvea Side Effect Report#8329969-X
Haemoptysis, Pulmonary Alveolar Haemorrhage
This Haemoptysis side effect was reported by a health professional from Italy. A 39-year-old male patient (weight:NA) experienced the following symptoms/conditions: hypertension,cough.The patient was prescribed Karvea (drug dosage: Unk), which was initiated on
Mar 05, 2012. Concurrently used drugs:
  • Aspirin (Daily Dose 500 Mg)
.After starting to take Karvea the consumer reported adverse symptoms, such as: Haemoptysis, Pulmonary Alveolar HaemorrhageThese side effects may potentially be related to Karvea. The patient was hospitalized.
Karvea Side Effect Report#8054110-0
Cerebrovascular Accident
This is a report of a male patient (weight: NA) from Australia, suffering from the following health symptoms/conditions: NA, who was treated with Karvea (dosage: NA, start time:
Jun 29, 2006), combined with:
  • Bicor
  • Lasix
  • Pradaxa (300 Mg)
  • Zyloprim
and developed a serious reaction and side effect(s): Cerebrovascular Accident after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Karvea treatment in male patients, resulting in Cerebrovascular Accident side effect. The patient was hospitalized.
Karvea Side Effect Report#7963095-4
Post Procedural Haemorrhage, Gastroenteritis Norovirus, Lymphocyte Percentage Decreased, Haematocrit Decreased, Red Blood Cell Count Decreased, Haemoglobin Decreased
This report suggests a potential Karvea Post Procedural Haemorrhage side effect(s) that can have serious consequences. A male patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: hypertension,diabetes mellitus and used Karvea (dosage: Dose Not Provided) starting NS. After starting Karvea the patient began experiencing various side effects, including: Post Procedural Haemorrhage, Gastroenteritis Norovirus, Lymphocyte Percentage Decreased, Haematocrit Decreased, Red Blood Cell Count Decreased, Haemoglobin DecreasedAdditional drugs used concurrently:
  • Berlinsulin H
  • Liprolog (Unit: E/ml)
  • Simvastatin (Dose Not Provided,scheduled As 1 X 1/2)
  • Trimineurin (Scheduling 1 X 1/2, 1 X 1/4.)
  • Xeloda (Dose Reduced In Response To Gastroenteritis Novovirus)
  • Digitoxin Tab
  • Memantine Hydrochloride (Dose Not Provided)
  • Oxaliplatin (Given On Days 1, 8, 15, 22 + 29. Last Dose Prior To 1st Sae 08/nov/2010. Actual Dose: 827mg)
The patient was hospitalized. Although Karvea demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Post Procedural Haemorrhage, may still occur.
Karvea Side Effect Report#7920208
Hyperkalaemia, Bradycardia
This Hyperkalaemia problem was reported by a consumer or non-health professional from IT. A 88-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On
Apr 07, 2009 this consumer started treatment with Karvea Film-coated Tabs 150 Mg (dosage: 1 Unit). The following drugs were being taken at the same time:
  • Moduretic (1df:5mg Plus 50mg Tabs?int On 7apr11)
  • Carvedilol (Int On 7apr11)
  • Cordarone (Int On 7apr11)
  • Zyloric (1df:300 Units Nos?scored Tabs)
  • Cardioaspirin (Gastroresistant Tabs?1 Unit)
  • Cardura (1 Unit)
  • Casodex (Film Coated Oral Tabs:1 Unit)
When using Karvea Film-coated Tabs 150 Mg, the patient experienced the following unwanted symptoms/side effects: Hyperkalaemia, BradycardiaThe 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 Hyperkalaemia, may become evident only after a product is in use by the general population.
Karvea Side Effect Report#7917799-X
Gastroenteritis Norovirus, Post Procedural Haemorrhage
This Gastroenteritis Norovirus side effect was reported by a consumer or non-health professional from Germany. A male patient (weight:NA) experienced the following symptoms/conditions: hypertension,rectal cancer.The patient was prescribed Karvea (drug dosage: Dose Not Provided), which was initiated on NS. Concurrently used drugs:
  • Xeloda (Last Dose Prior To Sae 09 November 2010. Dose Reduced)
  • Oxaliplatin (Dose: 50 Mg/m2, On D1, 8, 15, 22 And 29.last Dose Prior To Sae 08 Nov 2010.actual Dose 827mg.)
  • Digitoxin Tab
  • Trimineurin (Scheduling 1 X 1/2, 1 X 1/4.)
  • Berlinsulin H
  • Memantine Hydrochloride (Dose Not Provided)
  • Simvastatin (Dose Not Provided,scheduled As 1 X 1/2)
.After starting to take Karvea the consumer reported adverse symptoms, such as: Gastroenteritis Norovirus, Post Procedural HaemorrhageThese side effects may potentially be related to Karvea. The patient was hospitalized.
Karvea Side Effect Report#7903979-6
This is a report of a 64-year-old male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: NA, who was treated with Karvea (dosage: 1/ Tablet Per Day, start time:
Mar 02, 2009), combined with:
  • Levothyroxine Sodium
  • Ramipril
  • Torsemide
  • Protaphane
  • Radedorm
  • Aspirin
  • Tramadol Hcl (Daily Dose 150mg)
  • Omeprazole
and developed a serious reaction and side effect(s): after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Karvea treatment in male patients, resulting in Death side effect.
Karvea Side Effect Report#7743465-X
Lung Neoplasm, Presyncope
This report suggests a potential Karvea Lung Neoplasm side effect(s) that can have serious consequences. A male patient (weight: NA) from Australia was diagnosed with the following symptoms/conditions: NA and used Karvea (dosage: Unk) starting
Jan 01, 1998. After starting Karvea the patient began experiencing various side effects, including: Lung Neoplasm, PresyncopeAdditional drugs used concurrently:
  • Buprenorphine
  • Acetylsalicylic Acid Srt (Unk)
  • Pravastatin Sodium (Unk)
  • Nexium /01479303/ (Unk)
  • Buprenorphine
  • Buprenorphine (5 Mcg, Q1h)
  • Buprenorphine
  • Spiriva (Unk)
Although Karvea demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Lung Neoplasm, may still occur.
Karvea Side Effect Report#7372557-2
Blood Sodium Decreased
This Blood Sodium Decreased problem was reported by a consumer or non-health professional from Australia. A 83-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On
Jan 01, 2006 this consumer started treatment with Karvea (dosage: NA). The following drugs were being taken at the same time: NA. When using Karvea, the patient experienced the following unwanted symptoms/side effects: Blood Sodium DecreasedAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Blood Sodium Decreased, may become evident only after a product is in use by the general population.
Karvea Side Effect Report#7330255-5
Respiratory Failure, Asthenia, Renal Failure Acute, Hepatic Failure
This Respiratory Failure side effect was reported by a consumer or non-health professional from Italy. A 79-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Karvea Tabs 300 Mg (drug dosage: 1 Df: 1 Unit), which was initiated on
Jan 01, 2010. Concurrently used drugs:
  • Preterax (Preterax 2.5mg+0.625mg Tabs , 1 Unit/day.)
  • Humulin R
  • Novonorm
  • Imipenem
  • Metoprolol Tartrate
  • Permixon
  • Asa
.After starting to take Karvea Tabs 300 Mg the consumer reported adverse symptoms, such as: Respiratory Failure, Asthenia, Renal Failure Acute, Hepatic FailureThese side effects may potentially be related to Karvea Tabs 300 Mg. The patient was hospitalized.
Karvea Side Effect Report#7303778-2
Intestinal Obstruction, Neoplasm Malignant
This is a report of a male patient (weight: NA) from Australia, suffering from the following health symptoms/conditions: NA, who was treated with Karvea (dosage: NA, start time:
Oct 01, 2008), combined with:
  • Frusemide
  • Cetuximab
  • Carvedilol
  • Clexane
  • Xeloda (Dosing 12000 Mg/m2/d. Form And Route Per Protocol.)
  • Xeloda (Cycle No.:13. Number Of Days Taken:14 Days)
  • Fluorouracil
  • Avastin
and developed a serious reaction and side effect(s): Intestinal Obstruction, Neoplasm Malignant after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Karvea treatment in male patients, resulting in Intestinal Obstruction side effect.
Karvea Side Effect Report#7225668-6
Mobility Decreased, Cardiac Failure, Tinnitus, Angina Pectoris
This report suggests a potential Karvea Tabs 150 Mg Mobility Decreased side effect(s) that can have serious consequences. A 70-year-old female patient (weight: NA) from Germany was diagnosed with the following symptoms/conditions: hypertension and used Karvea Tabs 150 Mg (dosage: NA) starting
Jan 01, 1998. After starting Karvea Tabs 150 Mg the patient began experiencing various side effects, including: Mobility Decreased, Cardiac Failure, Tinnitus, Angina PectorisAdditional drugs used concurrently: NA. Although Karvea Tabs 150 Mg demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Mobility Decreased, may still occur.
Karvea Side Effect Report#7169953-5
Angina Pectoris, Cardiac Failure, Mobility Decreased, Tinnitus
This Angina Pectoris problem was reported by a consumer or non-health professional from Germany. A 70-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On
Jan 01, 1998 this consumer started treatment with Karvea Tabs 150 Mg (dosage: NA). The following drugs were being taken at the same time: NA. When using Karvea Tabs 150 Mg, the patient experienced the following unwanted symptoms/side effects: Angina Pectoris, Cardiac Failure, Mobility Decreased, TinnitusAlthough all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as Angina Pectoris, may become evident only after a product is in use by the general population.
Karvea Side Effect Report#7150197-8
Angina Pectoris, Cardiac Failure, Left Ventricular Hypertrophy, Mobility Decreased, Tinnitus
This Angina Pectoris side effect was reported by a physician from Germany. A 70-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Karvea Tabs 150 Mg (drug dosage: NA), which was initiated on
Jan 01, 1998. Concurrently used drugs: NA..After starting to take Karvea Tabs 150 Mg the consumer reported adverse symptoms, such as: Angina Pectoris, Cardiac Failure, Left Ventricular Hypertrophy, Mobility Decreased, TinnitusThese side effects may potentially be related to Karvea Tabs 150 Mg.
Karvea Side Effect Report#6942324-X
Anaemia, Hepatitis Acute
This is a report of a 69-year-old male patient (weight: NA) from Germany, suffering from the following health symptoms/conditions: hypertension, who was treated with Karvea Tabs 300 Mg (dosage: NA, start time:
Aug 06, 2009), combined with:
  • Spironolactone (Form Tablets; Hexal.)
and developed a serious reaction and side effect(s): Anaemia, Hepatitis Acute after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Karvea Tabs 300 Mg treatment in male patients, resulting in Anaemia side effect. The patient was hospitalized.


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The appearance of Karvea 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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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.

    Karvea 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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