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Slow-K (Potassium) - Reports of Side Effects & Adverse Reactions

 



This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Slow-K (Potassium). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.

Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.

All cases (28)
     Blood Potassium Decreased (10)Muscle Spasms (5)Blood Pressure Increased (4)more >>

Cases resulting in a serious event (28)
     Blood Potassium Decreased (10)Muscle Spasms (5)Blood Pressure Increased (4)more >>

Cases resulting in death (4)
     Lung Abscess (2)Interstitial Lung Disease (2)Pseudomonas Infection (1)more >>

Cases resulting in life threatening events (3)
     Neutrophil Count Increased (2)Alanine Aminotransferase Increased (2)Blood Lactate Dehydrogenase Increased (2)more >>

Cases resulting in hospitalization (12)
     Blood Potassium Decreased (4)Cardiac Operation (3)Surgery (3)more >>

Cases resulting in disability (1)
     Gastrointestinal Haemorrhage (1)Renal Impairment (1)

Cases resulting in other serious reactions (19)
     Blood Potassium Decreased (10)Muscle Spasms (5)Blood Pressure Increased (4)more >>

Below is a sample of reports where side effects / adverse reactions may be related to Slow-K (Potassium). For a complete list and/or a specific selection of reports, please use the links in the index above.

Adverse event in male receiving Slow-K (Potassium)

Reported by a physician from Japan on 2007-10-30

Patient: male

Adverse reactions / side effects: Interstitial Lung Disease, Respiratory Failure, Lung Abscess

Adverse event resulted in: death

Suspect drug(s):
Biofermin R
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Erythrocin
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Ferromia
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Finibax

Finibax
    Indication: Lung Abscess

Itraconazole
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Juzen-Taiho-TO
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Mucosta
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Norvasc
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Slow-K
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Sucralfate
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Zantac
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Cravit



Adverse event in male receiving Slow-K (Potassium)

Reported by a physician from Japan on 2007-10-19

Patient: male

Adverse reactions / side effects: Interstitial Lung Disease, Lung Abscess

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Biofermin R
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Erythrocin Lactobionate
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Ferromia
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Finibax

Finibax
    Indication: Lung Abscess

Itraconazole
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Juzen-Taiho-TO
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Mucosta
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Norvasc
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Slow-K
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Sucralfate
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Zantac
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Other drugs received by patient: Levofloxacin



Adverse event in 84 year old receiving Slow-K (Potassium)

Reported by a individual with unspecified qualification from Australia on 2007-10-05

Patient: 84 year old

Adverse reactions / side effects: LIP Swelling, Rash

Adverse event resulted in: hospitalization

Suspect drug(s):
Slow-K (Potassium)



Adverse event in female receiving Slow-K (Potassium)

Reported by a pharmacist from Netherlands on 2007-07-09

Patient: female

Adverse reactions / side effects: Renal Impairment, Creatinine Renal Clearance Decreased

Suspect drug(s):
Slow-K (Potassium)

Other drugs received by patient: Isosorbide Dinitrate; Quinsapril; Diclofenac; Nitrazepam



Adverse event in 89 year old female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-05-25

Patient: 89 year old female, weighing 49.0 kg (107.8 pounds)

Adverse reactions / side effects: Urinary Tract Infection, Pseudomonas Infection, Arrhythmia, Surgery, Blood Potassium Decreased, Diarrhoea, Pulmonary Oedema, Hypertension, Respiratory Tract Infection

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Diovan
    Dosage: 80 mg, qd
    Administration route: Oral
    Indication: Hypertension

Slow-K
    Dosage: unk, tid
    Administration route: Oral
    Indication: Electrolyte Substitution Therapy

Trileptal
    Dosage: 150 mg/day
    Administration route: Oral
    Indication: Convulsion

Other drugs received by patient: Lamotrigine; Lasix; Motilium; Omeprazole; Ancoron; Anticoagulants



Adverse event in 60 year old male receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-05-25

Patient: 60 year old male

Adverse reactions / side effects: Coronary Artery Bypass, Oedema Peripheral, Cardiac Operation, Mitral Valve Repair, Pyrexia, Fluid Retention

Adverse event resulted in: hospitalization

Suspect drug(s):
Slow-K
    Dosage: 600 mg, bid
    Administration route: Oral
    Indication: Mineral Supplementation
    End date: 2007-04-21

Slow-K
    Dosage: 600 mg, qd
    Administration route: Oral
    Start date: 2007-05-01

Other drugs received by patient: Furosemide



Adverse event in 61 year old female receiving Slow-K (Potassium)

Reported by a physician from Brazil on 2007-05-11

Patient: 61 year old female, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Intestinal Adenocarcinoma, Intestinal Operation, Retching, Blood Potassium Decreased, Extrasystoles, Gastric Disorder

Suspect drug(s):
Higroton
    Dosage: 50 mg, unk
    Administration route: Oral
    Indication: Arrhythmia

Potassium Chloride

Slow-K
    Dosage: 2 df/day
    Administration route: Oral
    Indication: Blood Potassium Decreased

Other drugs received by patient: Atenolol; Simvacor



Adverse event in 60 year old male receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-05-11

Patient: 60 year old male

Adverse reactions / side effects: Coronary Artery Bypass, Oedema Peripheral, Cardiac Operation, Mitral Valve Repair, Pyrexia, Fluid Retention

Adverse event resulted in: hospitalization

Suspect drug(s):
Slow-K
    Dosage: 600 mg, bid
    Administration route: Oral
    Indication: Mineral Supplementation
    End date: 2007-04-21

Slow-K
    Dosage: 600 mg, qd
    Administration route: Oral
    Start date: 2007-05-01

Other drugs received by patient: Furosemide



Adverse event in 44 year old male receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-04-30

Patient: 44 year old male, weighing 73.0 kg (160.6 pounds)

Adverse reactions / side effects: Thyroid Operation, Blood Potassium Decreased

Suspect drug(s):
Potassium Chloride
    Dosage: 2 tablets/day
    Administration route: Oral
    Start date: 2007-04-14

Slow-K
    Dosage: 600 mg, bid
    Administration route: Oral
    Indication: Hypokalaemia

Slow-K
    Dosage: 600 mg, qd
    Start date: 2006-04-14

Other drugs received by patient: OS-CAL D; Synthroid



Adverse event in 81 year old female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-04-09

Patient: 81 year old female, weighing 60.0 kg (132.0 pounds)

Adverse reactions / side effects: Pruritus, Surgery, Blood Potassium Decreased, Therapy Responder, Rash, Emotional Disorder, Asthenia, Muscle Spasms

Adverse event resulted in: hospitalization

Suspect drug(s):
Slow-K (Potassium)

Other drugs received by patient: Inderal; Sertraline; Amiloride Hydrochloride



Adverse event in 61 year old female receiving Slow-K (Potassium)

Reported by a physician from Brazil on 2007-03-23

Patient: 61 year old female, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Intestinal Adenocarcinoma, Retching, Blood Potassium Decreased, Extrasystoles, Gastric Disorder

Suspect drug(s):
Higroton
    Dosage: 50 mg, unk
    Administration route: Oral
    Indication: Arrhythmia

Potassium Chloride

Slow-K
    Dosage: 2 df/day
    Administration route: Oral
    Indication: Blood Potassium Decreased

Other drugs received by patient: Atenolol; Simvacor



Adverse event in 48 year old male receiving Slow-K (Potassium)

Reported by a physician from Japan on 2007-03-23

Patient: 48 year old male

Adverse reactions / side effects: Gastrointestinal Haemorrhage, Renal Impairment

Adverse event resulted in: death, disablity

Suspect drug(s):
Allopurinol
    Administration route: Oral
    Indication: Hyperuricaemia
    Start date: 2006-09-05
    End date: 2006-12-19

Baraclude
    Administration route: Oral
    Indication: Hepatitis B
    Start date: 2006-12-05
    End date: 2007-01-08

Lasix
    Administration route: Oral
    Indication: Renal Disorder
    Start date: 2006-09-05
    End date: 2007-01-08

Micardis
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-09-05
    End date: 2006-12-19

Prednisolone
    Administration route: Oral
    Indication: Graft Versus Host Disease
    Start date: 2006-02-03
    End date: 2007-01-08

Slow-K
    Administration route: Oral
    Indication: Hypokalaemia
    Start date: 2006-09-13
    End date: 2006-12-19



Adverse event in 61 year old female receiving Slow-K (Potassium)

Reported by a physician from Brazil on 2007-03-20

Patient: 61 year old female, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Intestinal Adenocarcinoma, Retching, Extrasystoles, Treatment Noncompliance, Gastric Disorder, Incorrect Drug Administration Duration, Overdose, Blood Potassium Decreased

Suspect drug(s):
Higroton
    Dosage: 50 mg, unk
    Administration route: Oral

Potassium Chloride

Slow-K

Other drugs received by patient: Atenolol; Simvacor



Adverse event in 76 year old female receiving Slow-K (Potassium)

Reported by a health professional (non-physician/pharmacist) from Brazil on 2007-03-19

Patient: 76 year old female, weighing 55.0 kg (121.0 pounds)

Adverse reactions / side effects: Vomiting, Dysphagia, Cerebral Ischaemia, Arrhythmia, Cerebral Haemorrhage, Blood Glucose Decreased, Biliary Colic, Respiratory Failure, Blood Potassium Decreased, Dehydration, Blood Glucose Fluctuation, Blood Pressure Fluctuation

Suspect drug(s):
Potassium Chloride
    Indication: Electrolyte Substitution Therapy
    Start date: 2007-02-05

Slow-K
    Indication: Electrolyte Substitution Therapy
    Start date: 2007-03-07

Tegretol
    Dosage: 200 mg, qd
    Administration route: Oral
    Indication: Convulsion
    Start date: 2006-01-01

Other drugs received by patient: Insulin Human; Captopril; Macrodantina; Plavix; Indapamide; Digoxin; Omeprazole; Amplictil; Amitriptyline HCL



Adverse event in female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-03-13

Patient: female

Adverse reactions / side effects: Cardiac Operation

Adverse event resulted in: hospitalization

Suspect drug(s):
Slow-K (Potassium)



Adverse event in 61 year old female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-03-12

Patient: 61 year old female, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Intestinal Adenocarcinoma, Retching, Blood Potassium Decreased, Gastric Disorder

Suspect drug(s):
Higroton
    Dosage: 50 mg, unk
    Administration route: Oral

Potassium Chloride

Slow-K

Other drugs received by patient: Atenolol; Simvacor



Adverse event in 70 year old female receiving Slow-K (Potassium)

Reported by a physician from Japan on 2007-02-27

Patient: 70 year old female

Adverse reactions / side effects: Blood Bilirubin Increased, Neutrophil Count Increased, Body Temperature Increased, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Eosinophil Count Increased, Liver Disorder, Haematocrit Decreased, Gamma-Glutamyltransferase Increased, Heart Rate Increased, Aspartate Aminotransferase Increased, White Blood Cell Count Increased

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Slow-K (Potassium)

Other drugs received by patient: Cylock; Trandolapril; Lasix; Aldactone; Warfarin Sodium; Mexiletine Hydrochloride; Magnesium Oxide; Verapamil; Domperidone



Adverse event in 40 year old male receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-02-27

Patient: 40 year old male, weighing 112.0 kg (246.4 pounds)

Adverse reactions / side effects: Emotional Distress, Blood Potassium Decreased, Chest Pain, Tachycardia, Nervousness

Adverse event resulted in: hospitalization

Suspect drug(s):
Slow-K
    Dosage: 2400 mg/day
    Administration route: Oral
    Indication: Blood Potassium Decreased

Slow-K
    Dosage: 1200 mmg/day
    Administration route: Oral



Adverse event in 80 year old female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-02-27

Patient: 80 year old female, weighing 98.0 kg (215.6 pounds)

Adverse reactions / side effects: Thrombosis, Allergic Bronchitis, Pain, Bone Erosion, Walking AID User, Prosthesis Implantation, Oedema Peripheral, Muscle Spasms

Adverse event resulted in: hospitalization

Suspect drug(s):
Slow-K
    Dosage: 1200 mg, bid
    Administration route: Oral
    Indication: Muscle Spasms

Slow-K
    Dosage: 600 mg, bid
    Administration route: Oral

Other drugs received by patient: Norvasc; Furosemide; Venalot; Cinelide; Deocil



Adverse event in 70 year old female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-02-19

Patient: 70 year old female, weighing 67.0 kg (147.4 pounds)

Adverse reactions / side effects: Cerebrovascular Accident

Adverse event resulted in: hospitalization

Suspect drug(s):
Slow-K (Potassium)

Other drugs received by patient: Losartan Potassium; Furosemide



Adverse event in 92 year old female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-02-19

Patient: 92 year old female

Adverse reactions / side effects: Blood Pressure Increased, Hypoaesthesia, Feeling Abnormal, Muscle Twitching

Suspect drug(s):
Capoten
    Indication: Hypertension

Slow-K
    Dosage: 600 mg, qd
    Administration route: Oral
    Indication: Blood Potassium Decreased

Other drugs received by patient: Higroton; Aldomet



Adverse event in 65 year old female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-02-19

Patient: 65 year old female

Adverse reactions / side effects: Poor Quality Sleep, Blood Pressure Increased, Depression, Eye Disorder, Muscle Spasms, Nervousness

Suspect drug(s):
Slow-K (Potassium)

Other drugs received by patient: Lipitor; Cymbalta



Adverse event in 73 year old male receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-02-16

Patient: 73 year old male

Adverse reactions / side effects: Myalgia, Blood Pressure Increased, Angina Pectoris, Muscle Spasms

Suspect drug(s):
Slow-K (Potassium)



Adverse event in 65 year old female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-02-16

Patient: 65 year old female

Adverse reactions / side effects: Poor Quality Sleep, Blood Pressure Increased, Depression, Eye Disorder, Muscle Spasms, Nervousness

Suspect drug(s):
Slow-K (Potassium)

Other drugs received by patient: Lipitor; Cymbalta



Adverse event in 86 year old female receiving Slow-K (Potassium)

Reported by a consumer/non-health professional from Brazil on 2007-02-12

Patient: 86 year old female

Adverse reactions / side effects: Upper Limb Fracture, Cerebrovascular Disorder, Asthenia, Fall

Suspect drug(s):
Slow-K
    Indication: Blood Potassium Decreased
    Start date: 2007-02-01

Slow-K
    Dosage: 600 mg/day
    Administration route: Oral

Other drugs received by patient: Higroton

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