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Metamizole adverse events reported to FDA.

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Summary

FDA Adverse Reports: 12. View All

Metamizole FDA safety alerts: No

Reported deaths: 4

Reported hospitalizations: 7

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3Mouth Ulcers
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Often additional risks of using a medication, such as Metamizole, 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 Metamizole users, Learn more about unwanted side effects & find ways to reduce them. Browse Metamizole Adverse Reports reported to FDA and participate in Metamizole discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Metamizole. 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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Metamizole Adverse Effect Reports (FDA)

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6980195-6 | Overdose, Renal Impairment
on Aug 31, 2010 Female patient from ISRAEL , 15 years of age, was treated with Metamizole (View Usage). Patient experienced the following unwanted or unexpected effects: overdose, renal impairment. Metamizole dosage: 7 G, Unk. During the same period patient was treated with ACETAMINOPHEN (500 Mg, Unk) (View Acetaminophen Review and Acetaminophen Label ), CARBOCISTEINE (2.1 G, Unk) (View Carbocisteine Review and Carbocisteine Label ). Patient was hospitalized.

5482943-3 | Agranulocytosis, Gastritis Haemorrhagic, Haemorrhage Subcutaneous, Haemorrhagic Diathesis, Mucosal Haemorrhage, Pneumonia
Patient was taking Metamizole (View Usage). Patient had the following side effects: agranulocytosis, gastritis haemorrhagic, haemorrhage subcutaneous, haemorrhagic diathesis, mucosal haemorrhage, pneumonia (What is pneumonia?) on Oct 08, 2007 from Additional patient health information: Female patient , 81 years of age, was diagnosed with arthritis (What is arthritis?) and. Metamizole dosage: . During the same period patient was treated with METHOTREXATE (15 Mg/week) (View Methotrexate Review and Methotrexate Label ), DICLOFENAC SODIUM (View Diclofenac Sodium Review and Diclofenac Sodium Label ).

5465967-1 | Agranulocytosis, Ecchymosis, Gastritis Haemorrhagic, Haemorrhagic Diathesis, Mucosal Haemorrhage, Pneumonia
Adverse event was reported on Sep 21, 2007 by a Female patient taking Metamizole (View Usage) (Dosage: ) was diagnosed with arthritis (What is arthritis?) and. Location: , 81 years of age, After Metamizole was administered, patient had the following side effects: agranulocytosis, ecchymosis, gastritis haemorrhagic, haemorrhagic diathesis, mucosal haemorrhage, pneumonia (What is pneumonia?). During the same period patient was treated with METHOTREXATE (15 Mg/week) (View Methotrexate Review and Methotrexate Label ), DICLOFENAC (View Diclofenac Review and Diclofenac Label ).

5464514-8 | Coma, Grand Mal Convulsion, Hypertension, Hyponatraemia, Inappropriate Antidiuretic Hormone Secretion, Porphyria, Rhabdomyolysis
on Sep 14, 2007 Female patient from , 30 years of age, was diagnosed with abdominal pain (What is abdominal pain?), grand mal convulsion, nausea (What is nausea?) and was treated with Metamizole (View Usage). Patient experienced the following unwanted or unexpected effects: coma, grand mal convulsion, hypertension, hyponatraemia, inappropriate antidiuretic hormone secretion, porphyria, rhabdomyolysis. Metamizole dosage: . During the same period patient was treated with PARACETAMOL (View Paracetamol Review and Paracetamol Label ), DIAZEPAM (View Diazepam Review and Diazepam Label ), HYOSCINE N BUTYLBROMIDE (View Hyoscine N Butylbromide Review and Hyoscine N Butylbromide Label ), DICLOFENAC (View Diclofenac Review and Diclofenac Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ). Patient was hospitalized.


5442684-5 | Hyponatraemia, Inappropriate Antidiuretic Hormone Secretion
on Sep 04, 2007 Female patient from , 30 years of age, was diagnosed with hypertension and was treated with Metamizole (View Usage). Patient had the following side effects: hyponatraemia, inappropriate antidiuretic hormone secretion. Metamizole dosage: . During the same period patient was treated with DIAZEPAM (View Diazepam Review and Diazepam Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ), HYOSCINE N BUTYLBROMIDE (View Hyoscine N Butylbromide Review and Hyoscine N Butylbromide Label ), DICLOFENAC (View Diclofenac Review and Diclofenac Label ), HYDRALAZINE HCL (View Hydralazine Hcl Review and Hydralazine Hcl Label ). Patient was hospitalized.

5425387-2 | Confusional State, Reflexes Abnormal, Somnolence
Patient was taking Metamizole (View Usage). After Metamizole was administered, patient had the following side effects: confusional state, reflexes abnormal, somnolence on Aug 24, 2007 from Additional patient health information: Female patient , 77 years of age, . Metamizole dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), LACTULOSE (View Lactulose Review and Lactulose Label ), BARBITURATE (View Barbiturate Review and Barbiturate Label ), DOXEPIN HCL (View Doxepin Hcl Review and Doxepin Hcl Label ), ENALAPRIL (View Enalapril Review and Enalapril Label ), FLUNITRAZEPAM (View Flunitrazepam Review and Flunitrazepam Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

5425386-0 | Coma, Respiratory Failure
Adverse event was reported on Aug 24, 2007 by a Male patient taking Metamizole (View Usage) (Dosage: ) . Location: , 29 years of age, Patient experienced the following unwanted or unexpected effects: coma, respiratory failure. During the same period patient was treated with MORPHINE (View Morphine Review and Morphine Label ), ETILEFRINE (View Etilefrine Review and Etilefrine Label ), COCAINE (View Cocaine Review and Cocaine Label ), CODEINE SUL TAB (View Codeine Sul Tab Review and Codeine Sul Tab Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), HEROIN (View Heroin Review and Heroin Label ). Patient was hospitalized.

5425385-9 | Respiratory Failure
on Aug 24, 2007 Female patient from , 78 years of age, was treated with Metamizole (View Usage). Patient had the following side effects: respiratory failure. Metamizole dosage: . During the same period patient was treated with MIDAZOLAM HCL (View Midazolam Hcl Review and Midazolam Hcl Label ), DICLOFENAC (View Diclofenac Review and Diclofenac Label ), DOXYLAMINE (View Doxylamine Review and Doxylamine Label ), TRAMADOL HCL (View Tramadol Hcl Review and Tramadol Hcl Label ), PENTOBARBITAL CAP (View Pentobarbital Cap Review and Pentobarbital Cap Label ), METOPROLOL SUCCINATE (View Metoprolol Succinate Review and Metoprolol Succinate Label ). Patient was hospitalized.

5354671-6 | Bicytopenia, Candidiasis, Circulatory Collapse, Mouth Ulceration, Myelodysplastic Syndrome, Pharyngeal Ulceration, Pharyngolaryngeal Pain, Pneumonia, Staphylococcal Sepsis
on Jun 08, 2007 Female patient from , 76 years of age, was diagnosed with pain (What is pain?), rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Metamizole (View Usage). After Metamizole was administered, patient had the following side effects: bicytopenia, candidiasis, circulatory collapse, mouth ulceration, myelodysplastic syndrome, pharyngeal ulceration, pharyngolaryngeal pain, pneumonia (What is pneumonia?), staphylococcal sepsis. Metamizole dosage: . During the same period patient was treated with METHOTREXATE (View Methotrexate Review and Methotrexate Label ), STEROIDS (5 Mg Of Prednisone Equivalent) (View Steroids Review and Steroids Label ). Patient was hospitalized.

5236960-9 | Anaphylactic Shock
Patient was taking Metamizole (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock on Feb 07, 2007 from COLOMBIA Additional patient health information: Female patient , 18 years of age, . Metamizole dosage: . During the same period patient was treated with DICLOFENAC SODIUM (View Diclofenac Sodium Review and Diclofenac Sodium Label ).

5212270-0 | Agranulocytosis
Adverse event was reported on Jan 12, 2007 by a Male patient taking Metamizole (View Usage) (Dosage: ) . Location: , 37 years of age, Patient had the following side effects: agranulocytosis. During the same period patient was treated with CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label ), CEFIXIME CHEWABLE (View Cefixime Chewable Review and Cefixime Chewable Label ), CODEINE SUL TAB (View Codeine Sul Tab Review and Codeine Sul Tab Label ), ACETYLCYSTEINE (View Acetylcysteine Review and Acetylcysteine Label ).

5212261-X | Granulocytopenia, Hepatic Enzyme Decreased, Pyrexia
on Jan 12, 2007 Female patient from , 64 years of age, was diagnosed with pneumonia (What is pneumonia?) and was treated with Metamizole (View Usage). After Metamizole was administered, patient had the following side effects: granulocytopenia, hepatic enzyme decreased, pyrexia. Metamizole dosage: . During the same period patient was treated with CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label ), AMOXICILLIN/CLAVULANIC ACID (View Amoxicillin/clavulanic Acid Review and Amoxicillin/clavulanic Acid Label ), DESIPRAMINE HCL (View Desipramine Hcl Review and Desipramine Hcl Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).


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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 Metamizole 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 Metamizole quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Metamizole 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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Metamizole Reactions
Agranulocytosis
Anaphylactic Shock
Bicytopenia
Candidiasis
Circulatory Collapse
Coma
Confusional State
Ecchymosis
Gastritis Haemorrhagic
Grand Mal Convulsion
Granulocytopenia
Haemorrhage Subcutaneous
Haemorrhagic Diathesis
Hepatic Enzyme Decreased
Hypertension
Hyponatraemia
Inappropriate Antidiuretic Hormone Secretion
Mouth Ulceration
Mucosal Haemorrhage
Myelodysplastic Syndrome
Overdose
Pharyngeal Ulceration
Pharyngolaryngeal Pain
PneumoniaWhat is Pneumonia?
Porphyria
Pyrexia
Reflexes Abnormal
Renal Impairment
Respiratory Failure
Rhabdomyolysis
Metamizole 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 Metamizole 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!