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Common Aciclovir Side Effects

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Aciclovir adverse events reported to FDA.

Have You Experienced unusual Aciclovir symptoms? PatientsVille.com collects and analyzes Aciclovir side effect and adverse reports submitted by Aciclovir users, such as .

Summary

FDA Adverse Reports: 17. View All

Aciclovir FDA safety alerts: No

Reported deaths: 1

Reported hospitalizations: 2

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1Night Sweats, Generally Feeling Unwell
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Often additional risks of using a medication, such as Aciclovir, 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 Aciclovir users, Learn more about unwanted side effects & find ways to reduce them. Browse Aciclovir Adverse Reports reported to FDA and participate in Aciclovir discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Aciclovir. 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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Aciclovir Adverse Effect Reports (FDA)

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7005673-5 | Abdominal Pain, Diarrhoea, Intestinal Perforation, Renal Failure Acute, Vomiting
on Sep 15, 2010 Male patient from UNITED KINGDOM , 66 years of age, was treated with Aciclovir (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), diarrhoea, intestinal perforation, renal failure acute, vomiting. Aciclovir dosage: .

7005672-3 | Abdominal Pain, Acidosis, Intestinal Obstruction, Vomiting
Patient was taking Aciclovir (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), acidosis, intestinal obstruction, vomiting on Sep 15, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 36 years of age, . Aciclovir dosage: . During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ). Patient was hospitalized.

7002009-0 | Alanine Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Gamma-glutamyltransferase Increased, Hepatic Necrosis, Hepatitis, Liver Disorder, Liver Injury
Adverse event was reported on Sep 08, 2010 by a Female patient taking Aciclovir (View Usage) (Dosage: ) . Location: CHINA , 13 years of age, After Aciclovir was administered, patient had the following side effects: alanine aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, gamma-glutamyltransferase increased, hepatic necrosis, hepatitis (What is hepatitis?), liver disorder, liver injury. During the same period patient was treated with CEFRADINE (View Cefradine Review and Cefradine Label ).

7002007-7 | Alanine Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Chronic Hepatitis, Gamma-glutamyltransferase Increased, Liver Disorder, Liver Injury
on Sep 08, 2010 Female patient from CHINA , 34 years of age, was treated with Aciclovir (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, chronic hepatitis, gamma-glutamyltransferase increased, liver disorder, liver injury. Aciclovir dosage: . During the same period patient was treated with CEFRADINE (View Cefradine Review and Cefradine Label ).


6546151-7 | Eyelid Ptosis, Iiird Nerve Paralysis, Ivth Nerve Paralysis, Neuropathic Ulcer, Sight Disability, Trigeminal Palsy, Uveitis, Vith Nerve Paralysis
on Jan 11, 2010 Female patient from UNITED KINGDOM , child 9 years of age, was diagnosed with herpes zoster ophthalmic and was treated with Aciclovir (View Usage). Patient had the following side effects: eyelid ptosis, iiird nerve paralysis, ivth nerve paralysis, neuropathic ulcer, sight disability, trigeminal palsy, uveitis, vith nerve paralysis. Aciclovir dosage: . During the same period patient was treated with CEFTRIAXONE (View Ceftriaxone Review and Ceftriaxone Label ), FLOXACILLIN SODIUM (View Floxacillin Sodium Review and Floxacillin Sodium Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), TETRACAINE HYDROCHLORIDE (View Tetracaine Hydrochloride Review and Tetracaine Hydrochloride Label ). Patient was hospitalized.

6534612-6 | Aplasia Pure Red Cell, Arthralgia, Herpes Zoster
Patient was taking Aciclovir (View Usage). After Aciclovir was administered, patient had the following side effects: aplasia pure red cell, arthralgia, herpes zoster on Jan 06, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 54 years of age, weighting 95.90 lb, was diagnosed with herpes zoster and. Aciclovir dosage: . During the same period patient was treated with NEORECORMON (View Neorecormon Review and Neorecormon Label ), XENICAL (View Xenical Review and Xenical Label ), ENALAPRIL (View Enalapril Review and Enalapril Label ), CALCICHEW (View Calcichew Review and Calcichew Label ), ALFACALCIDOL (View Alfacalcidol Review and Alfacalcidol Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ).

6529055-5 | Neutropenia
Adverse event was reported on Jan 05, 2010 by a Male patient taking Aciclovir (View Usage) (Dosage: ) was diagnosed with burkitt's lymphoma and. Location: UNITED KINGDOM , 17 years of age, Patient experienced the following unwanted or unexpected effects: neutropenia. During the same period patient was treated with TRIMETHOPRIM + SULFAMETHOXAZOLE (View Trimethoprim + Sulfamethoxazole Review and Trimethoprim + Sulfamethoxazole Label ), DEXRAZOXANE (View Dexrazoxane Review and Dexrazoxane Label ), DOXORUBICIN HCL (View Doxorubicin Hcl Review and Doxorubicin Hcl Label ), METHOTREXATE SODIUM (View Methotrexate Sodium Review and Methotrexate Sodium Label ), PREDNISOLONE AND PREDNISOLONE STEAGLATE (View Prednisolone And Prednisolone Steaglate Review and Prednisolone And Prednisolone Steaglate Label ), VINCRISTINE SULFATE (View Vincristine Sulfate Review and Vincristine Sulfate Label ), CYCLOPHOSPHAMIDE (View Cyclophosphamide Review and Cyclophosphamide Label ), ETOPOSIDE (View Etoposide Review and Etoposide Label ).

6527755-4 | Hyponatraemia, Neutropenia, Renal Impairment
on Dec 23, 2009 Male patient from UNITED STATES , 24 years of age, was treated with Aciclovir (View Usage). Patient had the following side effects: hyponatraemia, neutropenia, renal impairment. Aciclovir dosage: . During the same period patient was treated with FAMCICLOVIR (Unk) (View Famciclovir Review and Famciclovir Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ), ANTI THYMOCYTE GLOBULIN NOS (View Anti-thymocyte Globulin Nos Review and Anti-thymocyte Globulin Nos Label ).

6527754-2 | Hyponatraemia, Neutropenia, Renal Impairment
on Dec 23, 2009 Female patient from UNITED STATES , 44 years of age, was diagnosed with graft versus host disease and was treated with Aciclovir (View Usage). After Aciclovir was administered, patient had the following side effects: hyponatraemia, neutropenia, renal impairment. Aciclovir dosage: . During the same period patient was treated with FAMCICLOVIR (Unk) (View Famciclovir Review and Famciclovir Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

6527698-6 | Hyponatraemia, Neutropenia, Renal Impairment
Patient was taking Aciclovir (View Usage). Patient experienced the following unwanted or unexpected effects: hyponatraemia, neutropenia, renal impairment on Dec 23, 2009 from UNITED STATES Additional patient health information: Female patient , 47 years of age, was diagnosed with graft versus host disease and. Aciclovir dosage: . During the same period patient was treated with FOSCARNET (Unk) (View Foscarnet Review and Foscarnet Label ), TACROLIMUS (Unk) (View Tacrolimus Review and Tacrolimus Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), MYCOPHENOLATE MOFETIL (View Mycophenolate Mofetil Review and Mycophenolate Mofetil Label ).

6527696-2 | Hyponatraemia, Neutropenia, Renal Impairment
Adverse event was reported on Dec 23, 2009 by a Female patient taking Aciclovir (View Usage) (Dosage: ) was diagnosed with graft versus host disease and. Location: UNITED STATES , 37 years of age, Patient had the following side effects: hyponatraemia, neutropenia, renal impairment. During the same period patient was treated with FOSCARNET (Unk) (View Foscarnet Review and Foscarnet Label ), CIDOFOVIR (5 Mg/kg, 1/week) (View Cidofovir Review and Cidofovir Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ).

6527693-7 | Hyponatraemia, Neutropenia, Renal Impairment
on Dec 23, 2009 Female patient from UNITED STATES , 55 years of age, was diagnosed with graft versus host disease and was treated with Aciclovir (View Usage). After Aciclovir was administered, patient had the following side effects: hyponatraemia, neutropenia, renal impairment. Aciclovir dosage: . During the same period patient was treated with FOSCARNET (Unk) (View Foscarnet Review and Foscarnet Label ), TACROLIMUS (Unk) (View Tacrolimus Review and Tacrolimus Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), MYCOPHENOLATE MOFETIL (View Mycophenolate Mofetil Review and Mycophenolate Mofetil Label ).

6526325-1 | Hyponatraemia, Neutropenia, Renal Impairment
on Dec 22, 2009 Female patient from UNITED STATES , 37 years of age, was diagnosed with graft versus host disease and was treated with Aciclovir (View Usage). Patient experienced the following unwanted or unexpected effects: hyponatraemia, neutropenia, renal impairment. Aciclovir dosage: . During the same period patient was treated with FOSCARNET (Unk) (View Foscarnet Review and Foscarnet Label ), CIDOFOVIR (5 Mg/kg, 1/week) (View Cidofovir Review and Cidofovir Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ).

6526319-6 | Hyponatraemia, Neutropenia, Renal Impairment
Patient was taking Aciclovir (View Usage). Patient had the following side effects: hyponatraemia, neutropenia, renal impairment on Dec 22, 2009 from UNITED STATES Additional patient health information: Female patient , 55 years of age, was diagnosed with graft versus host disease and. Aciclovir dosage: . During the same period patient was treated with FOSCARNET (Unk) (View Foscarnet Review and Foscarnet Label ), TACROLIMUS (Unk) (View Tacrolimus Review and Tacrolimus Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), MYCOPHENOLATE MOFETIL (View Mycophenolate Mofetil Review and Mycophenolate Mofetil Label ).

6526318-4 | Hyponatraemia, Neutropenia, Renal Impairment
Adverse event was reported on Dec 22, 2009 by a Female patient taking Aciclovir (View Usage) (Dosage: ) was diagnosed with graft versus host disease and. Location: UNITED STATES , 47 years of age, After Aciclovir was administered, patient had the following side effects: hyponatraemia, neutropenia, renal impairment. During the same period patient was treated with FOSCARNET (Unk) (View Foscarnet Review and Foscarnet Label ), TACROLIMUS (Unk) (View Tacrolimus Review and Tacrolimus Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), MYCOPHENOLATE MOFETIL (View Mycophenolate Mofetil Review and Mycophenolate Mofetil Label ).

6526317-2 | Hyponatraemia, Neutropenia, Renal Impairment
on Dec 22, 2009 Female patient from UNITED STATES , 44 years of age, was diagnosed with graft versus host disease and was treated with Aciclovir (View Usage). Patient experienced the following unwanted or unexpected effects: hyponatraemia, neutropenia, renal impairment. Aciclovir dosage: . During the same period patient was treated with FAMCICLOVIR (Unk) (View Famciclovir Review and Famciclovir Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

6526316-0 | Hyponatraemia, Neutropenia, Renal Impairment
on Dec 22, 2009 Male patient from UNITED STATES , 24 years of age, was treated with Aciclovir (View Usage). Patient had the following side effects: hyponatraemia, neutropenia, renal impairment. Aciclovir dosage: . During the same period patient was treated with FAMCICLOVIR (Unk) (View Famciclovir Review and Famciclovir Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ), ANTI THYMOCYTE GLOBULIN NOS (View Anti-thymocyte Globulin Nos Review and Anti-thymocyte Globulin Nos Label ).


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Aciclovir Questions, Answers, Feedback and Comments

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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 Aciclovir 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 Aciclovir quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Aciclovir 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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Aciclovir Reactions
Abdominal PainWhat is Abdominal pain?
Acidosis
Alanine Aminotransferase Increased
Aplasia Pure Red Cell
Arthralgia
Blood Alkaline Phosphatase Increased
Blood Bilirubin Increased
Chronic Hepatitis
Diarrhoea
Eyelid Ptosis
Gamma-glutamyltransferase Increased
Hepatic Necrosis
HepatitisWhat is Hepatitis?
Herpes Zoster
Hyponatraemia
Iiird Nerve Paralysis
Intestinal Obstruction
Intestinal Perforation
Ivth Nerve Paralysis
Liver Disorder
Liver Injury
Neuropathic Ulcer
Neutropenia
ParalysisWhat is Paralysis?
Renal Failure Acute
Renal Impairment
Sight Disability
Trigeminal Palsy
Uveitis
Vomiting
Aciclovir 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 Aciclovir 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!