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Indinavir adverse events reported to FDA.

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Summary

FDA Adverse Reports: 5. View All

Indinavir FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 2

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

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5444042-6 | Abortion Spontaneous
on Aug 23, 2007 Female patient from UNITED STATES , 34 years of age, was diagnosed with hiv infection (What is hiv infection?) and was treated with Indinavir (View Usage). Patient experienced the following unwanted or unexpected effects: abortion spontaneous. Indinavir dosage: . During the same period patient was treated with LAMIVUDINE (View Lamivudine Review and Lamivudine Label ), STAVUDINE (View Stavudine Review and Stavudine Label ).

5322494-X | Premature Baby, Small For Dates Baby
Patient was taking Indinavir (View Usage). Patient had the following side effects: premature baby, small for dates baby on May 07, 2007 from UNITED STATES Additional patient health information: Female patient , weighting 6.61 lb, . Indinavir dosage: . During the same period patient was treated with ZIDOVUDINE (View Zidovudine Review and Zidovudine Label ), LAMIVUDINE (View Lamivudine Review and Lamivudine Label ).

5322490-2 | Premature Baby, Small For Dates Baby
Adverse event was reported on May 07, 2007 by a Female patient taking Indinavir (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 4.41 lb, After Indinavir was administered, patient had the following side effects: premature baby, small for dates baby. During the same period patient was treated with ZIDOVUDINE (View Zidovudine Review and Zidovudine Label ), LAMIVUDINE (View Lamivudine Review and Lamivudine Label ).

5312435-3 | Blood Creatinine Increased, Retroviral Rebound Syndrome
on Apr 17, 2007 Female patient from SWEDEN , 15 years of age, was diagnosed with human immunodeficiency virus transmission and was treated with Indinavir (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, retroviral rebound syndrome. Indinavir dosage: . During the same period patient was treated with ZIDOVUDINE (View Zidovudine Review and Zidovudine Label ), STAVUDINE (View Stavudine Review and Stavudine Label ), LAMIVUDINE (View Lamivudine Review and Lamivudine Label ), RITONAVIR (View Ritonavir Review and Ritonavir Label ). Patient was hospitalized.


5017501-8 | Nephrolithiasis
on Jun 01, 2006 Male patient from UNITED STATES , 67 years of age, weighting 185.0 lb, was treated with Indinavir (View Usage). Patient had the following side effects: nephrolithiasis. Indinavir dosage: . 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 Indinavir 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 Indinavir quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Indinavir 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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How Did You Deal with Side Effects?

During the same period patient was treated with ATAZANAVIR SULFATE (View Atazanavir Sulfate Review and Atazanavir Sulfate Label ), INDINAVIR (View Indinavir Review and ...

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

Increasing the indinavir dose to 1000 mg every 8 hours does not compensate for the increased indinavir metabolism due to SUSTIVA. When indinavir at an increased dose ...

During the same period patient was treated with ZIDOVUDINE (View Zidovudine Review and Zidovudine Label ), INDINAVIR (View Indinavir Review and Indinavir Label ).

May decrease levels of indinavir (increase indinavir to 1g every 8 hours), amprenavir, atazanavir, clarithromycin, calcium channel blockers (eg, diltiazem, felodipine ...

... Lamivudine Review and Lamivudine Label ), STAVUDINE (View Stavudine Review and Stavudine Label ), INDINAVIR (View Indinavir Review and Indinavir Label ), SAQUINAVIR (View ...

INDINAVIR SULFATE (Caps) (View Indinavir Sulfate Review and Indinavir Sulfate Label ), LAMIVUDINE (View Lamivudine Review and Lamivudine Label ), ABACAVIR (View Abacavir ...

... include macrolide antibiotics (e.g., erythromycin, troleandomycin, clarithromycin), HIV protease or reverse transcriptase inhibitors (e.g., ritonavir, indinavir ...

May decrease levels of indinavir (increase indinavir to 1g every 8 hours), amprenavir, atazanavir, clarithromycin, calcium channel blockers (eg, diltiazem, felodipine ...

In patients who are taking TARCEVA with a strong CYP3A4 inhibitor such as, but not limited to, atazanavir, clarithromycin, indinavir, itraconazole, ketoconazole ...

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Indinavir Reactions
Abortion Spontaneous
Blood Creatinine Increased
Nephrolithiasis
Premature Baby
Retroviral Rebound Syndrome
Small For Dates Baby
Indinavir 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 Indinavir 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!