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Spektramox adverse events reported to FDA.

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Summary

FDA Adverse Reports: 10. View All

Spektramox FDA safety alerts: No

Reported hospitalizations: 8

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

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5579211-8 | Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Diarrhoea, Nausea, Ocular Icterus, Oral Pain, Pruritus, Transaminases Increased, Weight Decreased
on Dec 21, 2007 Female patient from SWEDEN , 62 years of age, was treated with Spektramox (View Usage). Patient experienced the following unwanted or unexpected effects: blood alkaline phosphatase increased, blood bilirubin increased, diarrhoea, nausea (What is nausea?), ocular icterus, oral pain, pruritus, transaminases increased, weight decreased. Spektramox dosage: 500mg Per Day. During the same period patient was treated with URSO FALK (View Urso Falk Review and Urso Falk Label ). Patient was hospitalized.

5450159-2 | International Normalised Ratio Increased, Retinal Haemorrhage, Visual Acuity Reduced
Patient was taking Spektramox (View Usage). Patient had the following side effects: international normalised ratio increased, retinal haemorrhage, visual acuity reduced on Aug 13, 2007 from DENMARK Additional patient health information: Female patient , 80 years of age, weighting 136.7 lb, . Spektramox dosage: . During the same period patient was treated with MAREVAN (View Marevan Review and Marevan Label ).

5311562-4 | Blood Bilirubin Increased, Jaundice, Liver Disorder, Nausea, Pruritus
Adverse event was reported on Apr 23, 2007 by a Male patient taking Spektramox (View Usage) (Dosage: 1.5g Per Day) . Location: SWEDEN , 69 years of age, After Spektramox was administered, patient had the following side effects: blood bilirubin increased, jaundice (What is jaundice?), liver disorder, nausea (What is nausea?), pruritus.

5075808-2 | Cough, Fatigue, Thrombocytopenia, Vomiting, Weight Decreased
on Jun 29, 2006 Male patient from SWEDEN , child 1 years of age, was diagnosed with otitis media acute and was treated with Spektramox (View Usage). Patient experienced the following unwanted or unexpected effects: cough, fatigue, thrombocytopenia, vomiting, weight decreased. Spektramox dosage: 7.5ml Per Day. Patient was hospitalized.


5044502-6 | Cough, Fatigue, Red Blood Cell Count Decreased, Thrombocytopenia, Vomiting, Weight Decreased
on Jun 29, 2006 Male patient from SWEDEN , child 1 years of age, was diagnosed with otitis media acute and was treated with Spektramox (View Usage). Patient had the following side effects: cough, fatigue, red blood cell count decreased, thrombocytopenia, vomiting, weight decreased. Spektramox dosage: 7.5ml Per Day. Patient was hospitalized.

4696017-2 | Abdominal Pain, Blood Bilirubin Increased, Chromaturia, Faeces Pale, Nausea, Transaminases Increased, Urine Odour Abnormal
Patient was taking Spektramox (View Usage). After Spektramox was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), blood bilirubin increased, chromaturia, faeces pale, nausea (What is nausea?), transaminases increased, urine odour abnormal on May 05, 2005 from Additional patient health information: Female patient , 73 years of age, . Spektramox dosage: . During the same period patient was treated with BRICANYL (View Bricanyl Review and Bricanyl Label ), LEVAXIN (View Levaxin Review and Levaxin Label ), PULMICORT (View Pulmicort Review and Pulmicort Label ). Patient was hospitalized.

4696016-0 | Abdominal Pain, Blood Bilirubin Increased, Chromaturia, Faeces Pale, Nausea, Transaminases Increased, Urine Odour Abnormal
Adverse event was reported on Apr 29, 2005 by a Female patient taking Spektramox (View Usage) (Dosage: ) . Location: , 73 years of age, Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), blood bilirubin increased, chromaturia, faeces pale, nausea (What is nausea?), transaminases increased, urine odour abnormal. During the same period patient was treated with BRICANYL (View Bricanyl Review and Bricanyl Label ), LEVAXIN (View Levaxin Review and Levaxin Label ), PULMICORT (View Pulmicort Review and Pulmicort Label ). Patient was hospitalized.

4662742-2 | Abdominal Pain, Blood Bilirubin Increased, Chromaturia, Faeces Pale, Nausea, Transaminases Increased, Urine Odour Abnormal
on May 05, 2005 Female patient from , 73 years of age, was treated with Spektramox (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), blood bilirubin increased, chromaturia, faeces pale, nausea (What is nausea?), transaminases increased, urine odour abnormal. Spektramox dosage: . During the same period patient was treated with BRICANYL (View Bricanyl Review and Bricanyl Label ), LEVAXIN (View Levaxin Review and Levaxin Label ), PULMICORT (View Pulmicort Review and Pulmicort Label ). Patient was hospitalized.

4627142-X | Cholestasis, Decreased Appetite, Jaundice, Liver Disorder, Nausea, Pruritus, Weight Decreased
on Jun 29, 2004 Female patient from , 50 years of age, was diagnosed with infection (What is infection?) and was treated with Spektramox (View Usage). After Spektramox was administered, patient had the following side effects: cholestasis, decreased appetite, jaundice (What is jaundice?), liver disorder, nausea (What is nausea?), pruritus, weight decreased. Spektramox dosage: 1u Three Times Per Day. During the same period patient was treated with ZOLOFT (View Zoloft Review and Zoloft Label ), ESTRACOMB (View Estracomb Review and Estracomb Label ). Patient was hospitalized.

4625341-4 | Cholestasis, Decreased Appetite, Jaundice, Liver Disorder, Nausea, Pruritus, Weight Decreased
Patient was taking Spektramox (View Usage). Patient experienced the following unwanted or unexpected effects: cholestasis, decreased appetite, jaundice (What is jaundice?), liver disorder, nausea (What is nausea?), pruritus, weight decreased on Jun 29, 2004 from Additional patient health information: Female patient , 50 years of age, was diagnosed with infection (What is infection?) and. Spektramox dosage: 1u Three Times Per Day. During the same period patient was treated with ZOLOFT (View Zoloft Review and Zoloft Label ), ESTRACOMB (View Estracomb Review and Estracomb 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 Spektramox 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 Spektramox quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Spektramox 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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sotradecol Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: spektramox Episodes: 1: Diagnosed with major depression ...

spektramox Episodes: 1: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: spiriva Episodes: 4: Diagnosed with major depression.Side ...

spektramox Episodes: 3: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: spiriva Episodes: 7: Diagnosed with major depression.Side ...

spektramox Episodes: 4: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: sporanox Episodes: 3: Diagnosed with major depression.Side ...

spektramox Episodes: 3: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: strattera Episodes: 1: Diagnosed with major depression ...

... PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), GENTAMICIN (View Gentamicin Review and Gentamicin Label ), AMOXICILLIN CLAVULANIC ACID (SPEKTRAMOX ...

spektramox Episodes: 3: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: spiriva Episodes: 3: Diagnosed with major depression.Side ...

spektramox Episodes: 2: Diagnosed with major depression.Side effects: cardiac failure, myocarditis More: spironolactone Episodes: 4: Diagnosed with major ...

During the same period patient was treated with ELOPRAM DROPS, SPEKTRAMOX. Patient was hospitalized. Elopram Side Effects Report: 5248026-2,Abdominal Pain Lower, C ...

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Spektramox Reactions
Abdominal PainWhat is Abdominal pain?
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Cholestasis
Chromaturia
Cough
Decreased Appetite
Diarrhoea
Faeces Pale
Fatigue
International Normalised Ratio Increased
JaundiceWhat is Jaundice?
Liver Disorder
NauseaWhat is Nausea?
Ocular Icterus
Oral Pain
Pruritus
Red Blood Cell Count Decreased
Retinal Haemorrhage
Thrombocytopenia
Transaminases Increased
Urine Odour Abnormal
Visual Acuity Reduced
Vomiting
Weight Decreased
Spektramox 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 Spektramox 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!