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Primaquine adverse events reported to FDA.

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Summary

FDA Adverse Reports: 6. View All

Primaquine FDA safety alerts: No

Reported hospitalizations: 3

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

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5465424-2 | Diarrhoea, Glucose-6-phosphate Dehydrogenase Deficiency, Haemolytic Anaemia, Headache, Nausea, Pyrexia
on Sep 20, 2007 Male patient from UNITED STATES , 21 years of age, was diagnosed with prophylaxis and was treated with Primaquine (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, glucose-6-phosphate dehydrogenase deficiency, haemolytic anaemia, headache (What is headache?), nausea (What is nausea?), pyrexia. Primaquine dosage: Po. Patient was hospitalized.

5419238-X | Blister, Rash, Rash Papular, Rash Pruritic
Patient was taking Primaquine (View Usage). Patient had the following side effects: blister, rash (What is rash?), rash papular, rash pruritic on Aug 17, 2007 from UNITED STATES Additional patient health information: Male patient , 32 years of age, weighting 209.0 lb, was diagnosed with malaria prophylaxis and. Primaquine dosage: 15 Mg Daily.

5040050-8 | Eyelid Oedema, Rash Erythematous
Adverse event was reported on Jun 21, 2006 by a Male patient taking Primaquine (View Usage) (Dosage: 2 Tablets Daily) was diagnosed with malaria (What is malaria?) and. Location: CANADA , 29 years of age, After Primaquine was administered, patient had the following side effects: eyelid oedema, rash erythematous. During the same period patient was treated with RITALIN (Unk) (View Ritalin Review and Ritalin Label ). Patient was hospitalized.

4735600-2 | Blood Methaemoglobin Present
on Aug 01, 2005 Male patient from UNITED STATES , 56 years of age, weighting 91.93 lb, was diagnosed with pneumocystis jiroveci pneumonia and was treated with Primaquine (View Usage). Patient experienced the following unwanted or unexpected effects: blood methaemoglobin present. Primaquine dosage: 52.6 Po Qd. During the same period patient was treated with CLINDAMYCIN (View Clindamycin Review and Clindamycin Label ), ZOSYN (View Zosyn Review and Zosyn Label ), AZITHROMYCIN (View Azithromycin Review and Azithromycin Label ), FLUCONAZOLE (View Fluconazole Review and Fluconazole Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).


4678062-6 | Acute Respiratory Distress Syndrome, Anaemia, Barotrauma, Hypotension, Malaria, Malaria Prophylaxis, Pneumothorax
on May 19, 2005 Male patient from , 21 years of age, was treated with Primaquine (View Usage). Patient had the following side effects: acute respiratory distress syndrome, anaemia, barotrauma, hypotension, malaria (What is malaria?), malaria prophylaxis, pneumothorax. Primaquine dosage: . During the same period patient was treated with CHLOROQUINE PHOSPHATE (View Chloroquine Phosphate Review and Chloroquine Phosphate Label ). Patient was hospitalized.

4631148-4 | Blood Methaemoglobin Present, Oxygen Saturation Decreased
Patient was taking Primaquine (View Usage). After Primaquine was administered, patient had the following side effects: blood methaemoglobin present, oxygen saturation decreased on Apr 07, 2005 from Additional patient health information: Female patient , weighting 238.8 lb, was diagnosed with pneumocystis jiroveci pneumonia and. Primaquine dosage: 30mg Qd Oral. During the same period patient was treated with ERYTHROMYCIN (View Erythromycin Review and Erythromycin Label ), FLUCONAZOLE (View Fluconazole Review and Fluconazole Label ), FERROUS SULFATE TAB (View Ferrous Sulfate Tab Review and Ferrous Sulfate Tab Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), DOCUSATE SODIUM (View Docusate Sodium Review and Docusate Sodium Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide 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 Primaquine 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 Primaquine quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Primaquine 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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PRIMAQUINE (Unk) (View Primaquine Review and Primaquine Label ), MYLICON (Unk) (View Mylicon Review and Mylicon Label ), ACETAMINOPHEN (Unk) ... Macrobid dose and Macrobid ...

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During the same period patient was treated with PRIMAQUINE (1 Tablet -26.3 Mg- Once Daily Po) (View Primaquine Review and Primaquine Label ). Patient was hospitalized and ...

During the same period patient was treated with PRIMAQUINE 26.3 MG, DAILY FOR 16 DAYS (26.3 Mg, Daily For 16 Days) (View Primaquine 26.3 Mg, Daily For 16 Days Review and ...

During the same period patient was treated with PRIMAQUINE (2 Tablets Daily 1x14 Days Po) (View Primaquine Review and Primaquine Label ). 5494663-X | Depression, Fear ...

Cases of hemolytic anemia of the primaquine-sensitivity type have been induced by nitrofurantoin. Hemolysis appears to be linked to a glucose-6-phosphate dehydrogenase ...

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Study to Assess the Tolerability and Efficacy of Anacetrapib Co-administered ... Pharmacokinetic Study of Primaquine and Dihydroartemisinin-Piperaquine in Healthy Subjects

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Primaquine Reactions
Acute Respiratory Distress Syndrome
Anaemia
Barotrauma
Blister
Blood Methaemoglobin Present
Diarrhoea
Eyelid Oedema
Glucose-6-phosphate Dehydrogenase Deficiency
Haemolytic Anaemia
HeadacheWhat is Headache?
Hypotension
MalariaWhat is Malaria?
Malaria Prophylaxis
NauseaWhat is Nausea?
Oxygen Saturation Decreased
Pneumothorax
Pyrexia
RashWhat is Rash?
Rash Erythematous
Rash Papular
Rash Pruritic
Vomiting
Primaquine 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 Primaquine 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!