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Karvea Side Effects

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.

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.

Karvea Side Effects Reported to FDA

The following 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.


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.
Pancreatitis Acute
on Feb 18, 2014 Male from IT , 71 years of age, was diagnosed with and was treated with Karvea. Directly after, patient experienced the unwanted or unexpected Karvea side effects: pancreatitis acute. Karvea dosage: N/A.
Associated medications used:
  • Metformin Hydrochloride
  • Lansoprazole
  • Torvast
  • Cardirene
  • Altiazem
Patient was hospitalized.

Syncope
Patient was taking Karvea. Patient felt the following Karvea side effects: syncope on Feb 11, 2014 from IT Additional patient health information: Female , 80 years of age, . Karvea dosage: N/A.
Multiple prescriptions taken:
  • Lorazepam
  • Eutirox


Psychomotor Retardation, Hypoglycaemia
Adverse event was reported on Dec 23, 2013 by a Female taking Karvea (Dosage: Strength: 75 Mg) . Location: IT , 80 years of age, After Karvea was administered, patient encountered several Karvea side effects: psychomotor retardation, hypoglycaemia.
Multiple concurrent drugs taken:
  • Madopar
  • Torvast (Strength: 10 Mg)
  • Delecit (Strength: 400 Mg)
  • Exemestane (Strength: 25 Mg)
  • Lantus
  • Humalog
  • Pentoxifylline
Patient was hospitalized.

Blood Sodium Decreased, Syncope
on Jul 22, 2013 Female from DE , 70 years of age, was diagnosed with and was treated with Karvea. Directly after, patient experienced the unwanted or unexpected Karvea side effects: blood sodium decreased, syncope. Karvea dosage: N/A.
Associated medications used:
  • Eferox (Eferox 50 (l-thyroxine).)
Patient was hospitalized.


Palpitations, Dyspnoea, Cough, Flushing, Dysgeusia
on Mar 18, 2013 Female from DE , 72 years of age, weighting 174.2 lb, was diagnosed with and was treated with Karvea. Patient felt the following Karvea side effects: palpitations, dyspnoea, cough, flushing, dysgeusia. Karvea dosage: Central Pharmaceutical Number: 0647629, [v09/2014], 98 Tablets] 150 Mg 1-0-0.

Nodal Arrhythmia, Renal Failure Acute, Toxicity To Various Agents, Conduction Disorder, Bradycardia
Patient was taking Karvea. After Karvea was administered, patient encountered several Karvea side effects: nodal arrhythmia, renal failure acute, toxicity to various agents, conduction disorder, bradycardia on Mar 15, 2013 from IT Additional patient health information: Female , 72 years of age, weighting 110.2 lb, was diagnosed with and. Karvea dosage: N/A.
Multiple concurrent drugs taken:
  • Lanoxin
  • Aldactone
  • Tareg
  • Lasix
  • Libradin
  • Congescor
  • Solosa
  • Nitroderm (Die Patches)
Patient was hospitalized.

Dizziness, Tinnitus
Adverse event was reported on Dec 13, 2012 by a Male taking Karvea (Dosage: N/A) was diagnosed with and. Location: DE , 64 years of age, weighting 189.6 lb, Directly after, patient experienced the unwanted or unexpected Karvea side effects: dizziness, tinnitus.

Atrial Fibrillation, Hypokalaemia
on Nov 02, 2012 Male from DE , 63 years of age, was diagnosed with and was treated with Karvea. Patient felt the following Karvea side effects: atrial fibrillation, hypokalaemia. Karvea dosage: 1df:1/3 Of A Tab Daily.
Multiple prescriptions taken:
  • Kalinor
  • Sotalex


Gastrointestinal Infection, Salpingo-oophoritis
on Sep 06, 2012 Female from DE , 61 years of age, weighting 178.6 lb, was diagnosed with and was treated with Karvea. After Karvea was administered, patient encountered several Karvea side effects: gastrointestinal infection, salpingo-oophoritis. Karvea dosage: Jun2004-may2011: 150 Mg, Tabs.
Multiple concurrent drugs taken:
  • Azithromycin
  • Prajmalium Bitartrate (Tabs)
  • Levothyroxin (Tabs)


Renal Cell Carcinoma, Ovarian Mass, Joint Swelling, Oedema Peripheral
Patient was taking Karvea. Directly after, patient experienced the unwanted or unexpected Karvea side effects: renal cell carcinoma, ovarian mass, joint swelling, oedema peripheral on Jun 20, 2012 from AUSTRALIA Additional patient health information: Female , weighting 136.7 lb, . Karvea dosage: N/A.
Associated medications used:
  • Pradaxa (220 Mg)
  • Crestor
  • Lasix
  • Protos


Acute Prerenal Failure, Nodal Arrhythmia
Adverse event was reported on May 23, 2012 by a Female taking Karvea (Dosage: 300 Mg) . Location: ITALY , 85 years of age, Patient felt the following Karvea side effects: acute prerenal failure, nodal arrhythmia.
Multiple prescriptions taken:
  • 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)
Patient was hospitalized.

Haemoptysis, Pulmonary Alveolar Haemorrhage
on Apr 26, 2012 Male from ITALY , 39 years of age, was diagnosed with and was treated with Karvea. After Karvea was administered, patient encountered several Karvea side effects: haemoptysis, pulmonary alveolar haemorrhage. Karvea dosage: Unk.
Multiple concurrent drugs taken:
  • Aspirin (Daily Dose 500 Mg)
Patient was hospitalized.

Cerebrovascular Accident
on Jan 11, 2012 Male from AUSTRALIA , weighting 211.6 lb, was treated with Karvea. Directly after, patient experienced the unwanted or unexpected Karvea side effects: cerebrovascular accident. Karvea dosage: N/A.
Associated medications used:
  • Bicor
  • Lasix
  • Pradaxa (300 Mg)
  • Zyloprim
Patient was hospitalized.

Post Procedural Haemorrhage, Gastroenteritis Norovirus, Lymphocyte Percentage Decreased, Haematocrit Decreased, Red Blood Cell Count Decreased, Haemoglobin Decreased
Patient was taking Karvea. Patient felt the following Karvea side effects: post procedural haemorrhage, gastroenteritis norovirus, lymphocyte percentage decreased, haematocrit decreased, red blood cell count decreased, haemoglobin decreased on Nov 23, 2011 from GERMANY Additional patient health information: Male , weighting 181.0 lb, was diagnosed with and. Karvea dosage: Dose Not Provided.
Multiple prescriptions taken:
  • 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)
Patient was hospitalized.

Hyperkalaemia, Bradycardia
Adverse event was reported on May 16, 2013 by a Male taking Karvea Film-coated Tabs 150 Mg (Dosage: 1 Unit) . Location: IT , 88 years of age, After Karvea was administered, patient encountered several Karvea side effects: hyperkalaemia, bradycardia.
Multiple concurrent drugs taken:
  • 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)
Patient was hospitalized.

Gastroenteritis Norovirus, Post Procedural Haemorrhage
on Sep 29, 2011 Male from GERMANY , weighting 181.0 lb, was diagnosed with and was treated with Karvea. Directly after, patient experienced the unwanted or unexpected Karvea side effects: gastroenteritis norovirus, post procedural haemorrhage. Karvea dosage: Dose Not Provided.
Associated medications used:
  • 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)
Patient was hospitalized.


on Nov 03, 2011 Male from GERMANY , 64 years of age, weighting 194.0 lb, was treated with Karvea. . Karvea dosage: 1/ Tablet Per Day.
Multiple prescriptions taken:
  • Levothyroxine Sodium
  • Ramipril
  • Torsemide
  • Protaphane
  • Radedorm
  • Aspirin
  • Tramadol Hcl (Daily Dose 150mg)
  • Omeprazole


Lung Neoplasm, Presyncope
Patient was taking Karvea. After Karvea was administered, patient encountered several Karvea side effects: lung neoplasm, presyncope on Sep 02, 2011 from AUSTRALIA Additional patient health information: Male , weighting 176.4 lb, . Karvea dosage: Unk.
Multiple concurrent drugs taken:
  • Buprenorphine
  • Acetylsalicylic Acid Srt (Unk)
  • Pravastatin Sodium (Unk)
  • Nexium /01479303/ (Unk)
  • Buprenorphine
  • Buprenorphine (5 Mcg, Q1h)
  • Buprenorphine
  • Spiriva (Unk)


Blood Sodium Decreased
Adverse event was reported on Mar 21, 2011 by a Female taking Karvea (Dosage: N/A) was diagnosed with and. Location: AUSTRALIA , 83 years of age, weighting 156.5 lb, Directly after, patient experienced the unwanted or unexpected Karvea side effects: blood sodium decreased.

Respiratory Failure, Asthenia, Renal Failure Acute, Hepatic Failure
on Feb 25, 2011 Male from ITALY , 79 years of age, was treated with Karvea Tabs 300 Mg. Patient felt the following Karvea side effects: respiratory failure, asthenia, renal failure acute, hepatic failure. Karvea Tabs 300 Mg dosage: 1 Df: 1 Unit.
Multiple prescriptions taken:
  • Preterax (Preterax 2.5mg+0.625mg Tabs , 1 Unit/day.)
  • Humulin R
  • Novonorm
  • Imipenem
  • Metoprolol Tartrate
  • Permixon
  • Asa
Patient was hospitalized.

Intestinal Obstruction, Neoplasm Malignant
on Feb 15, 2011 Male from AUSTRALIA , weighting 152.1 lb, was treated with Karvea. After Karvea was administered, patient encountered several Karvea side effects: intestinal obstruction, neoplasm malignant. Karvea dosage: N/A.
Multiple concurrent drugs taken:
  • 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


Mobility Decreased, Cardiac Failure, Tinnitus, Angina Pectoris
Patient was taking Karvea Tabs 150 Mg. Directly after, patient experienced the unwanted or unexpected Karvea side effects: mobility decreased, cardiac failure, tinnitus, angina pectoris on Jan 12, 2011 from GERMANY Additional patient health information: Female , 70 years of age, weighting 149.9 lb, was diagnosed with and. Karvea Tabs 150 Mg dosage: N/A.

Angina Pectoris, Cardiac Failure, Mobility Decreased, Tinnitus
Adverse event was reported on Dec 14, 2010 by a Female taking Karvea Tabs 150 Mg (Dosage: N/A) was diagnosed with and. Location: GERMANY , 70 years of age, weighting 149.9 lb, Patient felt the following Karvea side effects: angina pectoris, cardiac failure, mobility decreased, tinnitus.

Angina Pectoris, Cardiac Failure, Left Ventricular Hypertrophy, Mobility Decreased, Tinnitus
on Dec 06, 2010 Female from GERMANY , 70 years of age, weighting 149.9 lb, was diagnosed with and was treated with Karvea Tabs 150 Mg. After Karvea was administered, patient encountered several Karvea side effects: angina pectoris, cardiac failure, left ventricular hypertrophy, mobility decreased, tinnitus. Karvea Tabs 150 Mg dosage: N/A.

Anaemia, Hepatitis Acute
on Aug 23, 2010 Male from GERMANY , 69 years of age, weighting 200.6 lb, was diagnosed with and was treated with Karvea Tabs 300 Mg. Directly after, patient experienced the unwanted or unexpected Karvea side effects: anaemia, hepatitis acute. Karvea Tabs 300 Mg dosage: N/A.
Associated medications used:
  • Spironolactone (Form Tablets; Hexal.)
Patient was hospitalized.

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Keep Track of Side Effects

Note Your Observations

It is really important to keep of your 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


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  • User Sign In
  • Register to track your side effects

  • 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.

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