KLOR-CON Side Effects

6856343-5 | Abdominal Pain Upper, Diarrhoea, Nausea, Product Formulation Issue
on Jul 15, 2010 Female patient from UNITED STATES , 25 years of age, weighting 134.0 lb, was diagnosed with familial periodic paralysis and was treated with Klor-con (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, diarrhoea, nausea (What is nausea?), product formulation issue. Klor-con dosage: 25-50 Meq As Needed Po - Only Used Once.

6745665-4 | Back Pain, Emphysema, Irritable Bowel Syndrome, Lip Exfoliation, Lip Pain, Lip Swelling, Pneumonia, Weight Decreased
Patient was taking Klor-con (View Usage). Patient had the following side effects: back pain (What is back pain?), emphysema, irritable bowel syndrome (What is irritable bowel syndrome?), lip exfoliation, lip pain, lip swelling, pneumonia (What is pneumonia?), weight decreased on May 17, 2010 from UNITED STATES Additional patient health information: Female patient , 84 years of age, weighting 94.20 lb, was diagnosed with mineral supplementation, hypertension, pancreatic insufficiency and. Klor-con dosage: . During the same period patient was treated with METOPROLOL (View Metoprolol Review and Metoprolol Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), CREON (View Creon Review and Creon Label ). Patient was hospitalized.

6428789-0 | Blood Magnesium Decreased, Blood Potassium Decreased, Malaise, Palpitations, Paraesthesia, Product Solubility Abnormal
Adverse event was reported on Oct 19, 2009 by a Female patient taking Klor-con (View Usage) (Dosage: 1 In 1 D, Oral, Alternating 10 Meq And 20 Meq, Qd, Oral) was diagnosed with mineral supplementation and. Location: UNITED STATES , 68 years of age, After Klor-con was administered, patient had the following side effects: blood magnesium decreased, blood potassium decreased, malaise, palpitations, paraesthesia, product solubility abnormal. During the same period patient was treated with DIOVAN HCT (View Diovan Hct Review and Diovan Hct Label ), CELEBREX (View Celebrex Review and Celebrex Label ), TRAZODONE HCL (View Trazodone Hcl Review and Trazodone Hcl Label ), PREMPRO (View Prempro Review and Prempro Label ), QUESTRAN (View Questran Review and Questran Label ). Patient was hospitalized.

6416167-X | Epistaxis, Gastritis, Oesophagitis, Pancreatitis
on Oct 01, 2009 Female patient from UNITED STATES , 76 years of age, was diagnosed with blood potassium decreased and was treated with Klor-con (View Usage). Patient experienced the following unwanted or unexpected effects: epistaxis, gastritis, oesophagitis, pancreatitis. Klor-con dosage: 2 In 1 D, Oral. During the same period patient was treated with PREVACID (View Prevacid Review and Prevacid Label ). Patient was hospitalized.


6340179-8 | Asthenia, Blood Potassium Decreased, Fall, Fatigue
on Aug 13, 2009 Female patient from UNITED STATES , 46 years of age, was diagnosed with blood potassium decreased and was treated with Klor-con (View Usage). Patient had the following side effects: asthenia, blood potassium decreased, fall (What is fall?), fatigue. Klor-con dosage: 10 Meq, Qd, Po. During the same period patient was treated with RANITIDINE (View Ranitidine Review and Ranitidine Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ). Patient was hospitalized.

6340178-6 | Dyspnoea, Product Coating Issue, Product Substitution Issue
Patient was taking Klor-con (View Usage). After Klor-con was administered, patient had the following side effects: dyspnoea, product coating issue, product substitution issue on Aug 13, 2009 from UNITED STATES Additional patient health information: Female patient , 82 years of age, was diagnosed with mineral supplementation and. Klor-con dosage: 10 Meq Qd, Po. During the same period patient was treated with FUROSEMIDE (START UNK, CONTIN.) (View Furosemide (start-unk, Contin.) Review and Furosemide (start-unk, Contin.) Label ), METOPROLOL (START UNK, CONTIN.) (View Metoprolol (start-unk, Contin.) Review and Metoprolol (start-unk, Contin.) Label ), AMIODARONE (START UNK, CONTIN.) (View Amiodarone (start-unk, Contin.) Review and Amiodarone (start-unk, Contin.) Label ), PLAVIX (START UNK, CONTIN.) (View Plavix (start-unk, Contin.) Review and Plavix (start-unk, Contin.) Label ), COUMADIN (START UNK, CONTIN.) (View Coumadin (start-unk, Contin.) Review and Coumadin (start-unk, Contin.) Label ), ADVAIR (START UNK, CONTIN.) (View Advair (start-unk, Contin.) Review and Advair (start-unk, Contin.) Label ), AMBIEN (START UNK, CONTIN.) (View Ambien (start-unk, Contin.) Review and Ambien (start-unk, Contin.) Label ). Patient was hospitalized.

6271885-1 | Appendicitis Perforated, Blood Potassium Decreased, Carbon Dioxide Increased, Coma, Dizziness, Gastroenteritis Viral, Multi-organ Failure, Pain
Adverse event was reported on Jun 25, 2009 by a Female patient taking Klor-con (View Usage) (Dosage: 8 Meq With Lunch, 16 Meq With Dinner, Po) was diagnosed with mineral supplementation and. Location: UNITED STATES , 90 years of age, Patient experienced the following unwanted or unexpected effects: appendicitis perforated, blood potassium decreased, carbon dioxide increased, coma, dizziness (What is dizziness?), gastroenteritis viral, multi-organ failure, pain (What is pain?). Patient was hospitalized.

6019878-3 | Asthenia, Blood Potassium Decreased, Fall
on Dec 04, 2008 Male patient from UNITED STATES , 66 years of age, was diagnosed with mineral supplementation and was treated with Klor-con (View Usage). Patient had the following side effects: asthenia, blood potassium decreased, fall (What is fall?). Klor-con dosage: 10 Meq, Bid; Po. During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), VITAMINS (View Vitamins Review and Vitamins Label ).

5875682-8 | Blood Potassium Decreased, Dizziness, Fatigue
on Aug 22, 2008 Female patient from UNITED STATES , 73 years of age, was diagnosed with mineral supplementation, blood pressure increased and was treated with Klor-con (View Usage). After Klor-con was administered, patient had the following side effects: blood potassium decreased, dizziness (What is dizziness?), fatigue. Klor-con dosage: 10 Meq, Bid, Po. During the same period patient was treated with HYDROCHLOROTHIAZIDE (Po) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), ATACAND (START UNK, CONTIN) (View Atacand (start-unk, Contin) Review and Atacand (start-unk, Contin) Label ), PROTONIX (START UNK, CONTIN.) (View Protonix (start-unk, Contin.) Review and Protonix (start-unk, Contin.) Label ). Patient was hospitalized.

5729064-X | Blood Potassium Decreased, Cardiac Flutter, Constipation, Hypertension, Palpitations, Transient Ischaemic Attack
Patient was taking Klor-con (View Usage). Patient experienced the following unwanted or unexpected effects: blood potassium decreased, cardiac flutter, constipation (What is constipation?), hypertension, palpitations, transient ischaemic attack on Apr 11, 2008 from UNITED STATES Additional patient health information: Female patient , 69 years of age, . Klor-con dosage: 20 Meq, Qd, Po. During the same period patient was treated with HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), PRAVACHOL (View Pravachol Review and Pravachol Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), CENTRUM (View Centrum Review and Centrum Label ), CALCIUMN WITH VITAMIN D (View Calciumn With Vitamin D Review and Calciumn With Vitamin D Label ). Patient was hospitalized.

5370073-0 | Cardiac Arrest, Hyperkalaemia, Overdose
Adverse event was reported on Mar 16, 2007 by a Female patient taking Klor-con (View Usage) (Dosage: 40 Meq, Tid, Po) was diagnosed with hypokalaemia and. Location: UNITED STATES , 61 years of age, weighting 140.0 lb, Patient had the following side effects: cardiac arrest (What is cardiac arrest?), hyperkalaemia, overdose. During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), COUMADIN (View Coumadin Review and Coumadin Label ), XANAX (View Xanax Review and Xanax Label ).

5002484-7 | Asthma, Blood Cholesterol Increased, Cardiac Disorder, Cerebrovascular Accident, Chest Pain, Constipation, Cystitis, Diverticulitis, Dizziness
on Oct 17, 2005 Male patient from UNITED STATES , 42 years of age, weighting 401.2 lb, was diagnosed with blood potassium decreased, gastrooesophageal reflux disease, diabetes mellitus, thrombosis, arthritis (What is arthritis?), oedema peripheral and was treated with Klor-con (View Usage). After Klor-con was administered, patient had the following side effects: asthma (What is asthma?), blood cholesterol increased, cardiac disorder, cerebrovascular accident, chest pain (What is chest pain?), constipation (What is constipation?), cystitis, diverticulitis, dizziness (What is dizziness?). Klor-con dosage: . During the same period patient was treated with NEXIUM (View Nexium Review and Nexium Label ), LANTUS (View Lantus Review and Lantus Label ), COUMADIN (View Coumadin Review and Coumadin Label ), NAPROXEN (View Naproxen Review and Naproxen Label ), VIOXX (View Vioxx Review and Vioxx Label ), INSULIN (View Insulin Review and Insulin Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized and became disabled.

4936766-1 | Alanine Aminotransferase Increased, Arthralgia, Atelectasis, Back Pain, Blood Alkaline Phosphatase Increased, Blood Glucose Increased, Bronchitis, Cardiac Failure Congestive, Cardiomegaly
on Oct 21, 2005 Female patient from UNITED STATES , 67 years of age, weighting 169.8 lb, was diagnosed with back pain (What is back pain?) and was treated with Klor-con (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, arthralgia, atelectasis, back pain (What is back pain?), blood alkaline phosphatase increased, blood glucose increased, bronchitis (What is bronchitis?), cardiac failure congestive, cardiomegaly. Klor-con dosage: . During the same period patient was treated with COREG (View Coreg Review and Coreg Label ), LIBRIUM (View Librium Review and Librium Label ), HUMULIN (View Humulin Review and Humulin Label ), VIOXX (View Vioxx Review and Vioxx Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), DEMADEX (View Demadex Review and Demadex Label ), MECLIZINE (View Meclizine Review and Meclizine Label ). Patient was hospitalized.

4919541-3 | Blood Cholesterol Increased, Cardiac Disorder, Cerebrovascular Accident, Chest Pain, Deep Vein Thrombosis, Dyspnoea, Hypoaesthesia, Myocardial Infarction, Obesity
Patient was taking Klor-con (View Usage). Patient had the following side effects: blood cholesterol increased, cardiac disorder, cerebrovascular accident, chest pain (What is chest pain?), deep vein thrombosis (What is deep vein thrombosis?), dyspnoea, hypoaesthesia, myocardial infarction, obesity (What is obesity?) on Oct 17, 2005 from UNITED STATES Additional patient health information: Male patient , 42 years of age, weighting 401.2 lb, was diagnosed with blood potassium decreased, gastrooesophageal reflux disease, diabetes mellitus, thrombosis, arthritis (What is arthritis?), oedema peripheral and. Klor-con dosage: . During the same period patient was treated with NEXIUM (View Nexium Review and Nexium Label ), LANTUS (View Lantus Review and Lantus Label ), COUMADIN (View Coumadin Review and Coumadin Label ), NAPROXEN (View Naproxen Review and Naproxen Label ), VIOXX (View Vioxx Review and Vioxx Label ), INSULIN (View Insulin Review and Insulin Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized and became disabled.