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Cephadol adverse events reported to FDA.

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Summary

FDA Adverse Reports: 6. View All

Cephadol FDA safety alerts: No

Reported deaths: 4

Reported hospitalizations: 6

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Often additional risks of using a medication, such as Cephadol, 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 Cephadol users, Learn more about unwanted side effects & find ways to reduce them. Browse Cephadol Adverse Reports reported to FDA and participate in Cephadol discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Cephadol. 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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Cephadol Adverse Effect Reports (FDA)

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5393335-X | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Blood Creatine Phosphokinase Increased, Blood Creatinine Increased, Blood Pressure Decreased, Blood Urea Increased, C-reactive Protein Increased, Dehydration
on Jul 19, 2007 Female patient from JAPAN , 66 years of age, weighting 119.0 lb, was diagnosed with dizziness (What is dizziness?), hyperuricaemia, nausea (What is nausea?), chronic myeloid leukaemia and was treated with Cephadol (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased, dehydration. Cephadol dosage: 3 Df/day. During the same period patient was treated with URALYT (6 Df/day) (View Uralyt Review and Uralyt Label ), ALLOPURINOL (300 Mg/day) (View Allopurinol Review and Allopurinol Label ), NOVAMIN (15 Mg/day) (View Novamin Review and Novamin Label ), TICLOPIDINE HCL (200 Mg/day) (View Ticlopidine Hcl Review and Ticlopidine Hcl Label ), MERISLON (18 Mg/day) (View Merislon Review and Merislon Label ), GLEEVEC (400 Mg/day) (View Gleevec Review and Gleevec Label ). Patient was hospitalized.

5387285-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Blood Creatine Phosphokinase Increased, Blood Creatinine Increased, Blood Pressure Decreased, Blood Urea Increased, C-reactive Protein Increased, Dehydration
Patient was taking Cephadol (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased, dehydration on Jul 11, 2007 from JAPAN Additional patient health information: Female patient , 66 years of age, weighting 119.0 lb, was diagnosed with dizziness (What is dizziness?), hyperuricaemia, nausea (What is nausea?), chronic myeloid leukaemia and. Cephadol dosage: 3 Df/day. During the same period patient was treated with URALYT (6 Df/day) (View Uralyt Review and Uralyt Label ), ALLOPURINOL (300 Mg/day) (View Allopurinol Review and Allopurinol Label ), NOVAMIN (15 Mg/day) (View Novamin Review and Novamin Label ), TICLOPIDINE HCL (200 Mg/day) (View Ticlopidine Hcl Review and Ticlopidine Hcl Label ), MERISLON (18 Mg/day) (View Merislon Review and Merislon Label ), GLEEVEC (400 Mg/day) (View Gleevec Review and Gleevec Label ). Patient was hospitalized.

5285106-X | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Blood Creatine Phosphokinase Increased, Blood Creatinine Increased, Blood Pressure Decreased, Blood Urea Increased, C-reactive Protein Increased, Dehydration
Adverse event was reported on Mar 28, 2007 by a Female patient taking Cephadol (View Usage) (Dosage: 3 Df/day) was diagnosed with dizziness (What is dizziness?), hyperuricaemia, nausea (What is nausea?), chronic myeloid leukaemia and. Location: JAPAN , 66 years of age, weighting 119.0 lb, After Cephadol was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased, dehydration. During the same period patient was treated with URALYT (6 Df/day) (View Uralyt Review and Uralyt Label ), ALLOPURINOL (300 Mg/day) (View Allopurinol Review and Allopurinol Label ), NOVAMIN (15 Mg/day) (View Novamin Review and Novamin Label ), TICLOPIDINE HCL (200 Mg/day) (View Ticlopidine Hcl Review and Ticlopidine Hcl Label ), MERISLON (18 Mg/day) (View Merislon Review and Merislon Label ), GLEEVEC (400 Mg/day) (View Gleevec Review and Gleevec Label ). Patient was hospitalized.

5153933-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Blood Creatine Phosphokinase Increased, Blood Creatinine Increased, Blood Pressure Decreased, Blood Urea Increased, C-reactive Protein Increased, Dehydration
on Oct 11, 2006 Female patient from JAPAN , 66 years of age, was diagnosed with dizziness (What is dizziness?), hyperuricaemia, nausea (What is nausea?), chronic myeloid leukaemia and was treated with Cephadol (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased, dehydration. Cephadol dosage: 3 Df/day. During the same period patient was treated with URALYT (6 Df/day) (View Uralyt Review and Uralyt Label ), ALLOPURINOL (300 Mg/day) (View Allopurinol Review and Allopurinol Label ), NOVAMIN (15 Mg/day) (View Novamin Review and Novamin Label ), PANALDINE (200 Mg/day) (View Panaldine Review and Panaldine Label ), MERISLON (18 Mg/day) (View Merislon Review and Merislon Label ), GLEEVEC (400 Mg/day) (View Gleevec Review and Gleevec Label ). Patient was hospitalized.


4811335-2 | Chest Pain, Coronary Arterial Stent Insertion, Electrocardiogram St Segment Depression, Myocardial Infarction
on Aug 05, 2005 Male patient from JAPAN , 69 years of age, weighting 160.9 lb, was diagnosed with dizziness (What is dizziness?), psychosomatic disease, hypertension, cerebral infarction, hypercholesterolaemia and was treated with Cephadol (View Usage). Patient had the following side effects: chest pain (What is chest pain?), coronary arterial stent insertion, electrocardiogram st segment depression, myocardial infarction. Cephadol dosage: . During the same period patient was treated with SOLANAX (View Solanax Review and Solanax Label ), BLOPRESS (View Blopress Review and Blopress Label ), MUNOBAL (View Munobal Review and Munobal Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LOCHOL (20 Mg, Qd) (View Lochol Review and Lochol Label ). Patient was hospitalized.

4743694-3 | Coronary Arterial Stent Insertion, Myocardial Infarction
Patient was taking Cephadol (View Usage). After Cephadol was administered, patient had the following side effects: coronary arterial stent insertion, myocardial infarction on Aug 05, 2005 from JAPAN Additional patient health information: Male patient , 69 years of age, weighting 160.9 lb, was diagnosed with dizziness (What is dizziness?), psychosomatic disease, hypertension, cerebral infarction, hypercholesterolaemia and. Cephadol dosage: . During the same period patient was treated with SOLANAX (View Solanax Review and Solanax Label ), BLOPRESS (View Blopress Review and Blopress Label ), MUNOBAL (View Munobal Review and Munobal Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LOCHOL (20 Mg, Qd) (View Lochol Review and Lochol Label ). Patient was hospitalized.


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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 Cephadol 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 Cephadol quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Cephadol 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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During the same period patient was treated with GABALON (Unk) (View Gabalon Review and Gabalon Label ), PLAVIX (View Plavix Review and Plavix Label ), CEPHADOL (Unk) (View ...

Sosegon Label ), NIPOLAZIN (Total Daily Dose: 3 Mg Unit Dose: 3 Mg) (View Nipolazin Review and Nipolazin Label ), CEPHADOL (View Cephadol Review and Cephadol Label ).

During the same period patient was treated with ALMARL (AROTINOLOL HYDROCHLORIDE) (5 Mg, 1 In 1 D, Oral), LOCHOL (FLUVASTATIN SODIUM), CEPHADOL (DIFENIDOL HYDROCHLORIDE), ...

Report a Drug Side Effect. ... This anonymous Drug Side Effect Survey has 13 questions and takes less than 2 minutes to complete.

... Sosegon Label ), NIPOLAZIN (Total Daily Dose: 3 Mg Unit Dose: 3 Mg) (View Nipolazin Review and Nipolazin Label ), CEPHADOL (View Cephadol Review and Cephadol Label ).

Cephadol Side Effects... NOVAMIN (15 Mg/day) (View Novamin Review and Novamin Label ), TICLOPIDINE HCL (200 Mg/day) (View Ticlopidine Hcl Review and Ticlopidine Hcl ...

)During the same period patient was treated with ISCOTIN, LENDORMIN, WASSER V GRAN., LANSOPRAZOLE, DIOVAN, BIOFERMIN, CEPHADOL. Patient was hospitalized and became disabled.

cephadol Episodes: 2: Diagnosed with dizziness , psychosomatic disease, hypertension, cerebral infarction, hypercholesterolaemia.Side effects: coronary arterial ...

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Cephadol Reactions
Alanine Aminotransferase Increased
Aspartate Aminotransferase Increased
Blood Bilirubin Increased
Blood Creatine Phosphokinase Increased
Blood Creatinine Increased
Blood Pressure Decreased
Blood Urea Increased
C-reactive Protein Increased
Chest PainWhat is Chest pain?
Coronary Arterial Stent Insertion
Dehydration
Electrocardiogram St Segment Depression
Myocardial Infarction
Cephadol 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 Cephadol 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!