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Kerlone adverse events reported to FDA.

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Summary

FDA Adverse Reports: 13. View All

Kerlone FDA safety alerts: No

Reported hospitalizations: 10

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Often additional risks of using a medication, such as Kerlone, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Kerlone users, Learn more about unwanted side effects & find ways to reduce them. Browse Kerlone Adverse Reports reported to FDA and participate in Kerlone discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Kerlone. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Kerlone Adverse Effect Reports (FDA)

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6642601-6 | Oedema Peripheral, Segmented Hyalinising Vasculitis, Urticaria
on Mar 15, 2010 Female patient from FRANCE , 47 years of age, was treated with Kerlone (View Usage). Patient experienced the following unwanted or unexpected effects: oedema peripheral, segmented hyalinising vasculitis, urticaria. Kerlone dosage: . During the same period patient was treated with LODOZ (View Lodoz Review and Lodoz Label ), IRBESARTAN (View Irbesartan Review and Irbesartan Label ). Patient was hospitalized.

6375809-8 | Hepatocellular Injury, Jaundice
Patient was taking Kerlone (View Usage). Patient had the following side effects: hepatocellular injury, jaundice (What is jaundice?) on Sep 16, 2009 from FRANCE Additional patient health information: Male patient , 49 years of age, was diagnosed with hypertension and. Kerlone dosage: Unk. Patient was hospitalized.

5476077-1 | Hallucinations, Mixed
Adverse event was reported on Sep 27, 2007 by a Female patient taking Kerlone (View Usage) (Dosage: ) was diagnosed with hypertension, atrial fibrillation (What is atrial fibrillation?) and. Location: FRANCE , weighting 132.3 lb, After Kerlone was administered, patient had the following side effects: hallucinations, mixed. During the same period patient was treated with PREVISCAN (3/4 Tablet At Bedtime) (View Previscan Review and Previscan Label ), IRBESARTAN (75 Mg) (View Irbesartan Review and Irbesartan Label ).

5421118-0 | Hallucinations, Mixed
on Jul 02, 2007 Female patient from FRANCE , 60 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Kerlone (View Usage). Patient experienced the following unwanted or unexpected effects: hallucinations, mixed. Kerlone dosage: .


5217496-8 | Retinal Artery Occlusion, Visual Acuity Reduced
on Jan 15, 2007 Female patient from FRANCE , 64 years of age, weighting 125.7 lb, was diagnosed with depression (What is depression?) and was treated with Kerlone (View Usage). Patient had the following side effects: retinal artery occlusion, visual acuity reduced. Kerlone dosage: 10 Mg. During the same period patient was treated with RIVOTRIL (Unk) (View Rivotril Review and Rivotril Label ), PIASCLEDINE (View Piascledine Review and Piascledine Label ), ARTHROTEC (2 Unit) (View Arthrotec Review and Arthrotec Label ), PROZAC (View Prozac Review and Prozac Label ).

5201455-5 | Bradycardia Foetal, Caesarean Section, Foetal Distress Syndrome, Foetal Growth Retardation, Hypoglycaemia Neonatal, Meconium Stain, Tricuspid Valve Incompetence
Patient was taking Kerlone (View Usage). After Kerlone was administered, patient had the following side effects: bradycardia foetal, caesarean section, foetal distress syndrome, foetal growth retardation, hypoglycaemia neonatal, meconium stain, tricuspid valve incompetence on Dec 27, 2006 from FRANCE Additional patient health information: Male patient , weighting 5.73 lb, . Kerlone dosage: . Patient was hospitalized.

4713377-4 | Atrial Flutter, Oedema Peripheral, Pericardial Effusion
Adverse event was reported on Jul 06, 2005 by a Female patient taking Kerlone (View Usage) (Dosage: ) . Location: FRANCE , 68 years of age, Patient experienced the following unwanted or unexpected effects: atrial flutter, oedema peripheral, pericardial effusion. During the same period patient was treated with MODOPAR (125 Mg Five Times A Day 625 Mg) (View Modopar Review and Modopar Label ), MODOPAR LP (View Modopar Lp Review and Modopar Lp Label ), MODOPAR DISPERSIBLE (View Modopar Dispersible Review and Modopar Dispersible Label ), CELANCE (View Celance Review and Celance Label ), FORLAX (20 G) (View Forlax Review and Forlax Label ), HEPTAMYL (4 Unit) (View Heptamyl Review and Heptamyl Label ), EFFEXOR (75 Mg) (View Effexor Review and Effexor Label ), XANAX (0.75 Mg) (View Xanax Review and Xanax Label ). Patient was hospitalized.

4707361-4 | Hypoxia, Pneumonitis
on Jun 03, 2005 Female patient from FRANCE , 74 years of age, weighting 176.4 lb, was diagnosed with hypertension, essential hypertension and was treated with Kerlone (View Usage). Patient had the following side effects: hypoxia, pneumonitis. Kerlone dosage: Unk. During the same period patient was treated with COTAREG (Unk) (View Cotareg Review and Cotareg Label ), FLECAINIDE ACETATE (Unk) (View Flecainide Acetate Review and Flecainide Acetate Label ). Patient was hospitalized.

4703215-8 | Dyspnoea, Hypocapnia, Hypoxia, Interstitial Lung Disease
on Jun 10, 2005 Female patient from , 74 years of age, weighting 176.4 lb, was diagnosed with hypertension, essential hypertension and was treated with Kerlone (View Usage). After Kerlone was administered, patient had the following side effects: dyspnoea, hypocapnia, hypoxia, interstitial lung disease. Kerlone dosage: . During the same period patient was treated with COTAREG (View Cotareg Review and Cotareg Label ), FLECAINE (View Flecaine Review and Flecaine Label ). Patient was hospitalized.

4694435-X | Dyspnoea, Hypocapnia, Hypoxia, Interstitial Lung Disease
Patient was taking Kerlone (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, hypocapnia, hypoxia, interstitial lung disease on Jun 10, 2005 from Additional patient health information: Female patient , 74 years of age, weighting 176.4 lb, was diagnosed with cardiac failure, essential hypertension and. Kerlone dosage: . During the same period patient was treated with COTAREG (View Cotareg Review and Cotareg Label ), FLECAINE (View Flecaine Review and Flecaine Label ). Patient was hospitalized.

4690733-4 | Pneumonitis
Adverse event was reported on Jun 03, 2005 by a Female patient taking Kerlone (View Usage) (Dosage: Unk) was diagnosed with cardiac failure, essential hypertension and. Location: , 74 years of age, weighting 176.4 lb, Patient had the following side effects: pneumonitis. During the same period patient was treated with COTAREG (Unk) (View Cotareg Review and Cotareg Label ), FLECAINE (Unk) (View Flecaine Review and Flecaine Label ). Patient was hospitalized.

4620911-1 | Cholestasis, Cytolytic Hepatitis, Hepatitis A
on Mar 10, 2005 Female patient from , 77 years of age, was diagnosed with hypertension, hypothyroidism and was treated with Kerlone (View Usage). After Kerlone was administered, patient had the following side effects: cholestasis, cytolytic hepatitis, hepatitis a (What is hepatitis a?). Kerlone dosage: 20 Mg Od. During the same period patient was treated with LEVOTHYROXINE SODIUM (100 Mcg Qd) (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), ALDACTAZINE (SPIRONOLACTONE, ALTIZIDE) TABLET 25 MG (12.5 Mg Od) (View Aldactazine - (spironolactone, Altizide) - Tablet - 25 Mg Review and Aldactazine - (spironolactone, Altizide) - Tablet - 25 Mg Label ), HEXAQUINE (QUININE, THIAMINE) TABLET 160 MG (2 Unit) (View Hexaquine - (quinine, Thiamine) - Tablet - 160 Mg Review and Hexaquine - (quinine, Thiamine) - Tablet - 160 Mg Label ). Patient was hospitalized.

4585403-7 | Acute Prerenal Failure, Dehydration, Hyperuricaemia, Interstitial Lung Disease
on Jan 26, 2005 Male patient from , 80 years of age, was diagnosed with cardiac failure chronic and was treated with Kerlone (View Usage). Patient experienced the following unwanted or unexpected effects: acute prerenal failure, dehydration, hyperuricaemia, interstitial lung disease. Kerlone dosage: 2.5 Mg Po. During the same period patient was treated with NU LOTAN (LOSARTAN POTASSIUM) (View Nu-lotan (losartan Potassium) Review and Nu-lotan (losartan Potassium) Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), BAYASPIRIN (ASPIRIN) (View Bayaspirin (aspirin) Review and Bayaspirin (aspirin) Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), DIART (AZOSEMIDE) (View Diart (azosemide) Review and Diart (azosemide) Label ). Patient was hospitalized.


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Kerlone Questions, Answers, Feedback and Comments

Comments to date: 2. Page 1 of 1.

Carole Langton   Location unknown

8:55pm on Wednesday, October 8th, 2008

PS I am also on other drugs as I have had breast cancer and am diabetic

Carole Langton   Location unknown

8:54pm on Wednesday, October 8th, 2008

I have been on Kerlone for about 4 months. Prior to that, amongst other drugs I was on Atenelol. I... read more »

To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Kerlone risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Kerlone quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Kerlone use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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... 1 Df, Qd) (View Tareg Review and Tareg Label ), PRACTAZIN (1 Df, Qd) (View Practazin Review and Practazin Label ), KERLONE (20 Mg, Qd) (View Kerlone Review and Kerlone Label ).

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During the same period patient was treated with COTAREG (Strength: Reported As 160/25.) (View Cotareg Review and Cotareg Label ), KERLONE (View Kerlone Review and Kerlone ...

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Kerlone Review and Kerlone Label ), METFORMIN (850 Mg, Qd) (View Metformin Review and Metformin Label ), ASPIRIN (75 Mg/day) ..... style="vertical-align:top;">

kerlone Episodes: 2: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: lapatinib Episodes: 1: Diagnosed with major depression.Side ...

Delursan Label ), KERLONE (View Kerlone Review and Kerlone Label ), ESOMEPRAZOLE (View Esomeprazole Review and Esomeprazole Label ), OSTRAM (View Ostram Review and Ostram ...

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Kerlone Reactions
Acute Prerenal Failure
Atrial Flutter
Bradycardia Foetal
Caesarean Section
Cholestasis
Cytolytic Hepatitis
Dehydration
Dyspnoea
Foetal Distress Syndrome
Foetal Growth Retardation
Hallucinations, Mixed
Hepatitis AWhat is Hepatitis a?
Hepatocellular Injury
Hyperuricaemia
Hypocapnia
Hypoglycaemia Neonatal
Hypoxia
Interstitial Lung Disease
JaundiceWhat is Jaundice?
Meconium Stain
Oedema Peripheral
Pericardial Effusion
Pneumonitis
Retinal Artery Occlusion
Segmented Hyalinising Vasculitis
Tricuspid Valve Incompetence
Urticaria
Visual Acuity Reduced
Kerlone Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Kerlone adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!