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Cytoxan adverse events reported to FDA.

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Summary

FDA Adverse Reports: 297. View All

Cytoxan FDA safety alerts: No

Reported deaths: 59

Reported hospitalizations: 151

Cytoxan Dosage, Warnings, Usage.

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1Sinus Congestion
2Cough
3Headache
4Bone Pain In My Lower Back And Legs
5Bone Pain In My Lower Back
6Legs
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Often additional risks of using a medication, such as Cytoxan, 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 Cytoxan users, Learn more about unwanted side effects & find ways to reduce them. Browse Cytoxan Adverse Reports reported to FDA and participate in Cytoxan discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Cytoxan. 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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Cytoxan Adverse Effect Reports (FDA)

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6020396-7 | Abdominal Infection, Diverticulitis, Intestinal Perforation, Peritonitis
on Dec 23, 2008 Female patient from UNITED STATES , 69 years of age, was diagnosed with breast cancer (What is breast cancer?) and was treated with Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal infection, diverticulitis, intestinal perforation, peritonitis. Cytoxan dosage: . During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ), ARIMIDEX (View Arimidex Review and Arimidex Label ), ERGOCALCIFEROL (View Ergocalciferol Review and Ergocalciferol Label ), CALCIUM PHOSPHATE (View Calcium Phosphate Review and Calcium Phosphate Label ), CALCIUM + VITAMIN D (View Calcium + Vitamin D Review and Calcium + Vitamin D Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), NEULASTA (View Neulasta Review and Neulasta Label ). Patient was hospitalized.

6020208-1 | Disease Progression, Lymphocyte Count Abnormal, Neutrophil Count Abnormal, White Blood Cell Count Abnormal
Patient was taking Cytoxan (View Usage). Patient had the following side effects: disease progression, lymphocyte count abnormal, neutrophil count abnormal, white blood cell count abnormal on Dec 23, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 81.35 lb, was diagnosed with ependymoma and. Cytoxan dosage: 75mg Qhs Other. During the same period patient was treated with CELEBREX (100mg Bid Other) (View Celebrex Review and Celebrex Label ), THALIDOMIDE (450mg Qd Other) (View Thalidomide Review and Thalidomide Label ), ZANTAC (View Zantac Review and Zantac Label ), MIRALAX (View Miralax Review and Miralax Label ), BACTRIM (View Bactrim Review and Bactrim Label ), LABETALOL (View Labetalol Review and Labetalol Label ). Patient was hospitalized.

5990012-9 | Lymphopenia, Neutropenia, Pyrexia, White Blood Cell Count Increased
Adverse event was reported on Dec 09, 2008 by a Male patient taking Cytoxan (View Usage) (Dosage: 75 Mg Qhs Other) was diagnosed with ependymoma and. Location: UNITED STATES , weighting 81.35 lb, After Cytoxan was administered, patient had the following side effects: lymphopenia, neutropenia, pyrexia, white blood cell count increased. During the same period patient was treated with CELEBREX (100mg Bid Other) (View Celebrex Review and Celebrex Label ), THALIDOMIDE (450mg Qd Other) (View Thalidomide Review and Thalidomide Label ), FENOFIBRATE (86 Mg Qd Other) (View Fenofibrate Review and Fenofibrate Label ), ZANTAC (View Zantac Review and Zantac Label ), MIRALAX (View Miralax Review and Miralax Label ), BACTRIM (View Bactrim Review and Bactrim Label ), LABETALOL HCL (View Labetalol Hcl Review and Labetalol Hcl Label ). Patient was hospitalized.

5947838-7 | Abdominal Infection, Diverticulitis, Intestinal Perforation, Peritonitis
on Nov 07, 2008 Female patient from UNITED STATES , 69 years of age, was diagnosed with breast cancer (What is breast cancer?) and was treated with Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal infection, diverticulitis, intestinal perforation, peritonitis. Cytoxan dosage: . During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ), ARIMIDEX (View Arimidex Review and Arimidex Label ), ERGOCALCIFEROL (View Ergocalciferol Review and Ergocalciferol Label ), CALCIUM PHOSPHATE (View Calcium Phosphate Review and Calcium Phosphate Label ), CALCIUM + VITAMIN D (View Calcium + Vitamin D Review and Calcium + Vitamin D Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), NEULASTA (View Neulasta Review and Neulasta Label ). Patient was hospitalized.


5941296-4 | Bone Pain, Cough, Dyspnoea, Eating Disorder, Haematocrit Decreased, Influenza, Nausea, Night Sweats
on Nov 03, 2008 Male patient from UNITED STATES , 60 years of age, weighting 174.0 lb, was diagnosed with non-hodgkin's lymphoma and was treated with Cytoxan (View Usage). Patient had the following side effects: bone pain, cough, dyspnoea, eating disorder (What is eating disorder?), haematocrit decreased, influenza, nausea (What is nausea?), night sweats. Cytoxan dosage: 3 Weeks Apart Iv Drip. During the same period patient was treated with VEPESID (3 Weeks Apart Iv Drip) (View Vepesid Review and Vepesid Label ). Patient was hospitalized.

5940619-X | Body Temperature Increased, Cough, Dyspnoea, Fatigue, Lower Respiratory Tract Inflammation, Red Blood Cell Count Decreased
Patient was taking Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: body temperature increased, cough, dyspnoea, fatigue, lower respiratory tract inflammation, red blood cell count decreased on Nov 03, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 190.0 lb, was diagnosed with breast cancer (What is breast cancer?) and. Cytoxan dosage: . During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ).

5920255-1 | Dehydration, Haematoma, Hypertension, Nausea, Syncope
Adverse event was reported on Oct 14, 2008 by a Female patient taking Cytoxan (View Usage) (Dosage: Reduced To 300 Mg/m*2 From Cyc 2.) was diagnosed with colorectal cancer (What is colorectal cancer?), pain (What is pain?), cough, vomiting and. Location: UNITED STATES , 34 years of age, Patient experienced the following unwanted or unexpected effects: dehydration, haematoma, hypertension, nausea (What is nausea?), syncope. During the same period patient was treated with ZYC300 (View Zyc300 Review and Zyc300 Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ROBITUSSIN AC (3 Dosage Forms = 3 Teaspoons) (View Robitussin Ac Review and Robitussin Ac Label ), HYDROCODONE + HOMATROPINE (View Hydrocodone + Homatropine Review and Hydrocodone + Homatropine Label ), REGLAN (View Reglan Review and Reglan Label ), COMPAZINE (View Compazine Review and Compazine Label ), CEPHALEXIN (View Cephalexin Review and Cephalexin Label ). Patient was hospitalized.

5876390-X | Hepatic Enzyme Increased
on Sep 09, 2008 Female patient from UNITED STATES , 29 years of age, weighting 186.0 lb, was treated with Cytoxan (View Usage). Patient had the following side effects: hepatic enzyme increased. Cytoxan dosage: 100 Mg Daily Po. Patient was hospitalized.

5868538-8 | Loss Of Consciousness
on Sep 02, 2008 Female patient from UNITED STATES , 61 years of age, was treated with Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: loss of consciousness. Cytoxan dosage: . During the same period patient was treated with AVONEX (View Avonex Review and Avonex Label ). Patient was hospitalized.

5849400-3 | Dehydration, Haematoma, Hypertension, Nausea, Syncope Vasovagal
Patient was taking Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: dehydration, haematoma, hypertension, nausea (What is nausea?), syncope vasovagal on Aug 15, 2008 from UNITED STATES Additional patient health information: Female patient , 34 years of age, was diagnosed with colorectal cancer (What is colorectal cancer?), pain (What is pain?), cough, vomiting and. Cytoxan dosage: Reduced To 300 Mg/m*2 From Cyc 2.. During the same period patient was treated with ZYC300 (View Zyc300 Review and Zyc300 Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ROBITUSSIN AC (3 Dosage Forms = 3 Teaspoons) (View Robitussin Ac Review and Robitussin Ac Label ), HYDROCODONE + HOMATROPINE (View Hydrocodone + Homatropine Review and Hydrocodone + Homatropine Label ), REGLAN (View Reglan Review and Reglan Label ), COMPAZINE (View Compazine Review and Compazine Label ). Patient was hospitalized.

5844820-5 | Interstitial Lung Disease
Adverse event was reported on Aug 12, 2008 by a Female patient taking Cytoxan (View Usage) (Dosage: Lot #: 7h574g-17mar08, 71575a-31mar08, 71578b-14apr08, 71575b-25apr08, 71575b-12may08) was diagnosed with breast cancer (What is breast cancer?) and. Location: UNITED STATES , 76 years of age, weighting 134.5 lb, Patient had the following side effects: interstitial lung disease. During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), NEULASTA (View Neulasta Review and Neulasta Label ), ARANESP (View Aranesp Review and Aranesp Label ), ALOXI (View Aloxi Review and Aloxi Label ), EMEND (View Emend Review and Emend Label ). Patient was hospitalized.

5832243-4 | Gastroenteritis, Hepatitis Acute, Mental Status Changes
on Jul 21, 2008 Female patient from UNITED STATES , 45 years of age, was diagnosed with breast cancer (What is breast cancer?), arthritis (What is arthritis?), back pain (What is back pain?), nausea (What is nausea?) and was treated with Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: gastroenteritis (What is gastroenteritis?), hepatitis acute, mental status changes. Cytoxan dosage: Initiated On 29aug06;ther.dur:39 Days. During the same period patient was treated with TAXOL (Dose Reduced To 130mg On 27nov06;delayed On 07nov2006 And Resumed On 27nov2006.) (View Taxol Review and Taxol Label ), ADRIAMYCIN PFS (Initiated On 29aug06;ther.dur:39 Days) (View Adriamycin Pfs Review and Adriamycin Pfs Label ), NEULASTA (Initiated On 30aug06) (View Neulasta Review and Neulasta Label ), BEVACIZUMAB (Initiated On 29aug06;ther.dur:57 Days. Interrupted On 07nov206 And Resumed On 27nov2006.) (View Bevacizumab Review and Bevacizumab Label ), PERCOCET (View Percocet Review and Percocet Label ), COMPAZINE (View Compazine Review and Compazine Label ), ANZEMET (View Anzemet Review and Anzemet Label ). Patient was hospitalized.

5832164-7 | Blood Creatinine Increased
on Jul 31, 2008 Female patient from UNITED STATES , 63 years of age, weighting 222.0 lb, was diagnosed with breast cancer (What is breast cancer?) and was treated with Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased. Cytoxan dosage: 1236 Mg Q 21 Days Iv Drip. During the same period patient was treated with TAXOTERE (155 Mg Q 21 Days Iv Drip) (View Taxotere Review and Taxotere Label ).

5831857-5 | Amnesia, Chest Discomfort, Dyspnoea, Fall, Flushing, Haematoma, Head Injury, Hypersensitivity, Loss Of Consciousness
Patient was taking Cytoxan (View Usage). Patient had the following side effects: amnesia, chest discomfort, dyspnoea, fall (What is fall?), flushing, haematoma, head injury, hypersensitivity, loss of consciousness on Jul 31, 2008 from UNITED STATES Additional patient health information: Female patient , 61 years of age, . Cytoxan dosage: 2nd Cycle On 23jun08.. During the same period patient was treated with DOCETAXEL (View Docetaxel Review and Docetaxel Label ), PEGFILGRASTIM (View Pegfilgrastim Review and Pegfilgrastim Label ). Patient was hospitalized.

5828680-4 | Interstitial Lung Disease
Adverse event was reported on Jul 22, 2008 by a Female patient taking Cytoxan (View Usage) (Dosage: Lot #: 7h574g-17mar08, 71575a-31mar08, 71578b-14apr08, 71575b-25apr08, 71575b-12may08.) was diagnosed with breast cancer (What is breast cancer?) and. Location: UNITED STATES , 76 years of age, weighting 134.5 lb, After Cytoxan was administered, patient had the following side effects: interstitial lung disease. During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), NEULASTA (View Neulasta Review and Neulasta Label ), ARANESP (View Aranesp Review and Aranesp Label ), ALOXI (View Aloxi Review and Aloxi Label ), EMEND (View Emend Review and Emend Label ). Patient was hospitalized.

5821598-2 | Interstitial Lung Disease
on Jul 15, 2008 Female patient from UNITED STATES , 76 years of age, was treated with Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: interstitial lung disease. Cytoxan dosage: Lot #: 7h574g-17mar08, 71575a-31mar08, 71578b-14apr08, 71575b-25apr08, 71575b-12may08.. Patient was hospitalized.

5818845-X | Gastroenteritis, Hepatitis Acute, Mental Status Changes
on Jul 21, 2008 Female patient from UNITED STATES , 45 years of age, was diagnosed with breast cancer (What is breast cancer?), arthritis (What is arthritis?), back pain (What is back pain?), nausea (What is nausea?) and was treated with Cytoxan (View Usage). Patient had the following side effects: gastroenteritis (What is gastroenteritis?), hepatitis acute, mental status changes. Cytoxan dosage: Initiated On 29aug06. During the same period patient was treated with TAXOL (Dose Reduced To 130mg/m2 On 27nov06) (View Taxol Review and Taxol Label ), ADRIAMYCIN PFS (Initiated On 29aug06) (View Adriamycin Pfs Review and Adriamycin Pfs Label ), NEULASTA (Initiated On 30aug06) (View Neulasta Review and Neulasta Label ), BEVACIZUMAB (Initiated On 29aug06) (View Bevacizumab Review and Bevacizumab Label ), PERCOCET (View Percocet Review and Percocet Label ), COMPAZINE (View Compazine Review and Compazine Label ), ANZEMET (View Anzemet Review and Anzemet Label ). Patient was hospitalized.

5809884-3 | Myocardial Infarction
Patient was taking Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: myocardial infarction on Jul 10, 2008 from UNITED STATES Additional patient health information: Female patient , 39 years of age, weighting 114.6 lb, was diagnosed with multiple sclerosis (What is multiple sclerosis?), convulsion, bladder disorder and. Cytoxan dosage: . During the same period patient was treated with REBIF (View Rebif Review and Rebif Label ), ZANAFLEX (View Zanaflex Review and Zanaflex Label ), KEPPRA (View Keppra Review and Keppra Label ), ROBAXIN (View Robaxin Review and Robaxin Label ), SANCTURA (View Sanctura Review and Sanctura Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), NEURONTIN (View Neurontin Review and Neurontin Label ).

5809471-7 | Myocardial Infarction
Adverse event was reported on Jul 10, 2008 by a Female patient taking Cytoxan (View Usage) (Dosage: ) was diagnosed with multiple sclerosis (What is multiple sclerosis?), convulsion, bladder disorder and. Location: UNITED STATES , 39 years of age, weighting 114.6 lb, Patient experienced the following unwanted or unexpected effects: myocardial infarction. During the same period patient was treated with REBIF (View Rebif Review and Rebif Label ), ZANAFLEX (View Zanaflex Review and Zanaflex Label ), KEPPRA (View Keppra Review and Keppra Label ), ROBAXIN (View Robaxin Review and Robaxin Label ), SANCTURA (View Sanctura Review and Sanctura Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), NEURONTIN (View Neurontin Review and Neurontin Label ).

5805397-3 | Atrial Fibrillation, Cardiotoxicity, Tachycardia
on Jul 08, 2008 Female patient from UNITED STATES , 31 years of age, weighting 149.9 lb, was diagnosed with breast cancer (What is breast cancer?) and was treated with Cytoxan (View Usage). Patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), cardiotoxicity, tachycardia. Cytoxan dosage: . During the same period patient was treated with ADRIAMYCIN PFS (View Adriamycin Pfs Review and Adriamycin Pfs Label ), DOCETAXEL (Initiated In Feb2008.solution For Infusion.reported Dosage 75mg/m2 Per Dose. 3 Cyc) (View Docetaxel Review and Docetaxel Label ), ZOFRAN (View Zofran Review and Zofran Label ), DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), EMEND (View Emend Review and Emend Label ), ATIVAN (View Ativan Review and Ativan Label ), NEULASTA (View Neulasta Review and Neulasta Label ), LEUPROLIDE ACETATE (View Leuprolide Acetate Review and Leuprolide Acetate Label ).

5787444-0 | Oedema Peripheral, Pain In Extremity, Phlebitis
on Jun 23, 2008 Female patient from UNITED STATES , 57 years of age, was diagnosed with breast cancer (What is breast cancer?) and was treated with Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: oedema peripheral, pain in extremity, phlebitis. Cytoxan dosage: Cycle1:18mar08-18mar08,dur:1day. Cycle2:08apr08-08apr08,dur:1day. Cycle3:28apr08-28apr08,dur:1day.. During the same period patient was treated with TAXOTERE (Cycle1:146mg,iv,18mar08-18mar08. Cycle2:146mg,iv,08apr08-08apr08. Cycle3:146mg,iv,28apr08-28apr08.) (View Taxotere Review and Taxotere Label ), ALOXI (View Aloxi Review and Aloxi Label ), DECADRON (View Decadron Review and Decadron Label ), ATIVAN (View Ativan Review and Ativan Label ), EMEND (View Emend Review and Emend Label ), PLAVIX (View Plavix Review and Plavix Label ), PROTONIX (View Protonix Review and Protonix Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

5750320-3 | Pain In Jaw
Patient was taking Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: pain in jaw on May 21, 2008 from UNITED STATES Additional patient health information: Female patient , 59 years of age, weighting 130.1 lb, was diagnosed with amyotrophic lateral sclerosis (What is amyotrophic lateral sclerosis?) and. Cytoxan dosage: 3000mg Over 1 Hour Daily X2 Days Iv Bolus.

5750319-7 | Blood Pressure Increased, Chest Pain, Infusion Related Reaction, Pain In Jaw
Adverse event was reported on May 21, 2008 by a Male patient taking Cytoxan (View Usage) (Dosage: 3300mg Over 1 Hour Daily X 2 Days Iv Drip) . Location: UNITED STATES , 56 years of age, weighting 136.7 lb, Patient had the following side effects: blood pressure increased, chest pain (What is chest pain?), infusion related reaction, pain in jaw.

5747404-2 | Dehydration, Haematoma, Hypertension, Nausea, Syncope Vasovagal
on May 21, 2008 Female patient from UNITED STATES , 34 years of age, was diagnosed with colorectal cancer (What is colorectal cancer?), pain (What is pain?), cough, vomiting and was treated with Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: dehydration, haematoma, hypertension, nausea (What is nausea?), syncope vasovagal. Cytoxan dosage: Reduced To 300 Mg/m*2 From Cyc 2.. During the same period patient was treated with ZYC300 (View Zyc300 Review and Zyc300 Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), ROBITUSSIN AC (3 Dosage Forms = 3 Teaspoons) (View Robitussin Ac Review and Robitussin Ac Label ), HYDROCODONE + HOMATROPINE (View Hydrocodone + Homatropine Review and Hydrocodone + Homatropine Label ), REGLAN (View Reglan Review and Reglan Label ), COMPAZINE (View Compazine Review and Compazine Label ). Patient was hospitalized.

5746554-4 | Febrile Neutropenia, Pneumocystis Jiroveci Pneumonia
on Mar 24, 2008 Male patient from UNITED STATES , 33 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: febrile neutropenia, pneumocystis jiroveci pneumonia. Cytoxan dosage: . During the same period patient was treated with VINCRISTINE SULFATE (View Vincristine Sulfate Review and Vincristine Sulfate Label ), ADRIAMYCIN PFS (View Adriamycin Pfs Review and Adriamycin Pfs Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), NEULASTA (View Neulasta Review and Neulasta Label ). Patient was hospitalized.

5746552-0 | Erythema, Skin Lesion
Patient was taking Cytoxan (View Usage). Patient had the following side effects: erythema, skin lesion on Mar 12, 2008 from UNITED STATES Additional patient health information: Female patient , 83 years of age, was diagnosed with breast cancer metastatic and. Cytoxan dosage: . During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), COZAAR (View Cozaar Review and Cozaar Label ), VYTORIN (View Vytorin Review and Vytorin Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ).

5746550-7 | Pregnancy
Adverse event was reported on Mar 04, 2008 by a Female patient taking Cytoxan (View Usage) (Dosage: Duration:1.5yr) . Location: UNITED STATES , 31 years of age, After Cytoxan was administered, patient had the following side effects: pregnancy (What is pregnancy?).

5746549-0 | Pruritus, Urticaria
on Feb 27, 2008 Female patient from UNITED STATES , 81 years of age, weighting 125.7 lb, was diagnosed with breast cancer (What is breast cancer?), multiple myeloma (What is multiple myeloma?) and was treated with Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: pruritus, urticaria. Cytoxan dosage: Started On 27-nov-2007.. During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), NEULASTA (View Neulasta Review and Neulasta Label ), KYTRIL (View Kytril Review and Kytril Label ), DECADRON (View Decadron Review and Decadron Label ), PEPCID (View Pepcid Review and Pepcid Label ), BENADRYL (View Benadryl Review and Benadryl Label ), CENTRUM SILVER (View Centrum Silver Review and Centrum Silver Label ).

5746548-9 | Urticaria
on Feb 27, 2008 Female patient from UNITED STATES , 80 years of age, weighting 132.3 lb, was diagnosed with breast cancer (What is breast cancer?) and was treated with Cytoxan (View Usage). Patient had the following side effects: urticaria. Cytoxan dosage: . During the same period patient was treated with TAXOTERE (Infusion) (View Taxotere Review and Taxotere Label ), NEULASTA (Duration - 4 Courses Every 3 Weeks) (View Neulasta Review and Neulasta Label ), KYTRIL (View Kytril Review and Kytril Label ), DECADRON (View Decadron Review and Decadron Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ATARAX (View Atarax Review and Atarax Label ), MAGIC MOUTHWASH (View Magic Mouthwash Review and Magic Mouthwash Label ), ZOFRAN (View Zofran Review and Zofran Label ).

5746545-3 | Fatigue
Patient was taking Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: fatigue on Jan 23, 2008 from UNITED STATES Additional patient health information: Female patient , 14 years of age, was diagnosed with brain neoplasm malignant and. Cytoxan dosage: . During the same period patient was treated with ETOPOSIDE (50 Mg Qod, 100 Mg Qod X 21 Days; Alternate Q 21 Days) (View Etoposide Review and Etoposide Label ), THALOMID (View Thalomid Review and Thalomid Label ), CELEBREX (View Celebrex Review and Celebrex Label ).

5746542-8 | Hypersensitivity
Adverse event was reported on Mar 13, 2008 by a Female patient taking Cytoxan (View Usage) (Dosage: ) was diagnosed with breast cancer (What is breast cancer?) and. Location: UNITED STATES , 37 years of age, weighting 125.7 lb, Patient experienced the following unwanted or unexpected effects: hypersensitivity. During the same period patient was treated with DOCETAXEL (View Docetaxel Review and Docetaxel Label ), DECADRON (21-oct-2007 To 22-oct-2007. Restarted 22-oct-2007.) (View Decadron Review and Decadron Label ), ALOXI (View Aloxi Review and Aloxi Label ), ZANTAC (View Zantac Review and Zantac Label ), BENADRYL (View Benadryl Review and Benadryl Label ), ATIVAN (View Ativan Review and Ativan Label ), EMEND (View Emend Review and Emend Label ).

5746540-4 | Disease Progression, Pneumonia
on Nov 29, 2007 Male patient from UNITED STATES , 62 years of age, was diagnosed with multiple myeloma (What is multiple myeloma?) and was treated with Cytoxan (View Usage). Patient had the following side effects: disease progression, pneumonia (What is pneumonia?). Cytoxan dosage: . During the same period patient was treated with REVLIMID (15mg/day On 1-14 Days + 22-28 Days. Addtl Lot#428564. 10mg/day From 14-may-2007-withdrawn.) (View Revlimid Review and Revlimid Label ), ACYCLOVIR SODIUM (View Acyclovir Sodium Review and Acyclovir Sodium Label ), BACTRIM (View Bactrim Review and Bactrim Label ), DEXAMETHASONE TAB (View Dexamethasone Tab Review and Dexamethasone Tab Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), VELCADE (View Velcade Review and Velcade Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ), SERTRALINE (View Sertraline Review and Sertraline Label ). Patient was hospitalized.

5746536-2 | Pancytopenia
on Nov 15, 2007 Female patient from UNITED STATES , 72 years of age, weighting 125.7 lb, was diagnosed with breast cancer (What is breast cancer?), anaemia of malignant disease and was treated with Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: pancytopenia. Cytoxan dosage: . During the same period patient was treated with PROCRIT (13jun07-06aug07 (55days) 40000 Units Once A Week And 13aug07-20aug07 60000 Units Once A Week.) (View Procrit Review and Procrit Label ), RITUXAN (View Rituxan Review and Rituxan Label ), FLUDARA (View Fludara Review and Fludara Label ).

5746533-7 | Sepsis
Patient was taking Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: sepsis (What is sepsis?) on Sep 13, 2007 from UNITED STATES Additional patient health information: Male patient , 32 years of age, . Cytoxan dosage: . Patient was hospitalized.

5746528-3 | Granulocytopenia, Leukopenia
Adverse event was reported on Aug 28, 2007 by a Female patient taking Cytoxan (View Usage) (Dosage: ) . Location: UNITED STATES , 73 years of age, Patient had the following side effects: granulocytopenia, leukopenia. During the same period patient was treated with VINCRISTINE (View Vincristine Review and Vincristine Label ).

5746523-4 | Abdominal Distension, Asthenia, Cough, Decreased Activity, Dysgeusia, Fatigue, Nausea, Rhinorrhoea
on Jul 25, 2007 Male patient from UNITED STATES , weighting 134.5 lb, was treated with Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: abdominal distension, asthenia, cough, decreased activity, dysgeusia, fatigue, nausea (What is nausea?), rhinorrhoea. Cytoxan dosage: . During the same period patient was treated with ADRIAMYCIN PFS (View Adriamycin Pfs Review and Adriamycin Pfs Label ), VINCRISTINE (View Vincristine Review and Vincristine Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), ALTACE (View Altace Review and Altace Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ).

5746518-0 | Leukaemia
on Jun 06, 2007 Female patient from UNITED STATES , 40 years of age, weighting 249.1 lb, was diagnosed with multiple sclerosis (What is multiple sclerosis?) and was treated with Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: leukaemia. Cytoxan dosage: . During the same period patient was treated with NOVANTRONE (View Novantrone Review and Novantrone Label ). Patient was hospitalized.

5746515-5 | White Blood Cell Count Decreased
Patient was taking Cytoxan (View Usage). Patient had the following side effects: white blood cell count decreased on Apr 05, 2007 from UNITED STATES Additional patient health information: Male patient , 65 years of age, was diagnosed with multiple myeloma (What is multiple myeloma?) and. Cytoxan dosage: . During the same period patient was treated with REVLIMID (View Revlimid Review and Revlimid Label ), VELCADE (View Velcade Review and Velcade Label ). Patient was hospitalized.

5739862-4 | Dyspnoea, Lung Disorder, Oxygen Saturation Decreased
Adverse event was reported on May 13, 2008 by a Male patient taking Cytoxan (View Usage) (Dosage: Every 4 Weeks Iv Drip) was diagnosed with lymphoma (What is lymphoma?) and. Location: UNITED STATES , 65 years of age, weighting 160.0 lb, After Cytoxan was administered, patient had the following side effects: dyspnoea, lung disorder, oxygen saturation decreased. During the same period patient was treated with ADRIAMYCIN PFS (View Adriamycin Pfs Review and Adriamycin Pfs Label ), VINCRISTINE (View Vincristine Review and Vincristine Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), RITUXAN (Every 4 Weeks Iv Drip) (View Rituxan Review and Rituxan Label ). Patient was hospitalized.

5693188-6 | Diarrhoea, Gastric Ulcer Haemorrhage
on Apr 01, 2008 Female patient from UNITED STATES , 65 years of age, was diagnosed with b-cell lymphoma, blood potassium decreased and was treated with Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, gastric ulcer haemorrhage. Cytoxan dosage: . During the same period patient was treated with DOXORUBICIN HCL (View Doxorubicin Hcl Review and Doxorubicin Hcl Label ), VINCRISTINE SULFATE (View Vincristine Sulfate Review and Vincristine Sulfate Label ), KLOR CON (1df-20meq Taken From 08feb To 06mar And 40meq From 07mar To 12mar08 And Adviced To Restart As 20meq.) (View Klor-con Review and Klor-con Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), DAPSONE (View Dapsone Review and Dapsone Label ), DIOVAN (View Diovan Review and Diovan Label ), FLUOXETINE (View Fluoxetine Review and Fluoxetine Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ). Patient was hospitalized.

5682461-3 | Febrile Neutropenia, Pneumocystis Jiroveci Pneumonia
on Mar 24, 2008 Male patient from UNITED STATES , 33 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with Cytoxan (View Usage). Patient had the following side effects: febrile neutropenia, pneumocystis jiroveci pneumonia. Cytoxan dosage: . During the same period patient was treated with VINCRISTINE SULFATE (View Vincristine Sulfate Review and Vincristine Sulfate Label ), ADRIAMYCIN PFS (View Adriamycin Pfs Review and Adriamycin Pfs Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), NEULASTA (View Neulasta Review and Neulasta Label ). Patient was hospitalized.

5616516-6 | Neutropenia, Overdose, Somnolence
Patient was taking Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: neutropenia, overdose, somnolence on Jan 30, 2008 from UNITED STATES Additional patient health information: Female patient , 34 years of age, was diagnosed with multiple sclerosis (What is multiple sclerosis?), anxiety (What is anxiety?) and. Cytoxan dosage: . During the same period patient was treated with ATIVAN (View Ativan Review and Ativan Label ), REBIF (Stopped On 30may07;restarted On 18jun07,dose:22mcg,3/1/wk,sc To Sep07.) (View Rebif Review and Rebif Label ), CORTICOSTEROID (View Corticosteroid Review and Corticosteroid Label ). Patient was hospitalized.

5614205-5 | Liver Function Test Abnormal, Neutropenia, Pyrexia, Urinary Tract Infection
Adverse event was reported on Jan 31, 2008 by a Female patient taking Cytoxan (View Usage) (Dosage: ) was diagnosed with breast cancer (What is breast cancer?), colony stimulating factor prophylaxis, insomnia, hypertension, mineral supplementation, arthralgia, peptic ulcer (What is peptic ulcer?) and. Location: UNITED STATES , 61 years of age, weighting 123.5 lb, Patient experienced the following unwanted or unexpected effects: liver function test abnormal, neutropenia, pyrexia, urinary tract infection (What is urinary tract infection?). During the same period patient was treated with ADRIAMYCIN PFS (Started On 17-oct-2008.dose Reduced To 45mg/m2 From 21nov2006) (View Adriamycin Pfs Review and Adriamycin Pfs Label ), BEVACIZUMAB (Started On 17-oct-2008) (View Bevacizumab Review and Bevacizumab Label ), NEULASTA (Started On 18-oct-2008) (View Neulasta Review and Neulasta Label ), AMBIEN (View Ambien Review and Ambien Label ), HYDROCHLOROTHIAZIDE (2 Tabs Every Day) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), POTASSIUM CHLORIDE (1 Dosage Form=1 Tab) (View Potassium Chloride Review and Potassium Chloride Label ), NAPROXEN (View Naproxen Review and Naproxen Label ), PREVACID (View Prevacid Review and Prevacid Label ). Patient was hospitalized.

5612498-1 | Liver Function Test Abnormal, Pyrexia
on Jan 31, 2008 Female patient from UNITED STATES , 61 years of age, weighting 123.5 lb, was diagnosed with breast cancer (What is breast cancer?), colony stimulating factor prophylaxis, insomnia, hypertension, mineral supplementation, arthralgia, peptic ulcer (What is peptic ulcer?) and was treated with Cytoxan (View Usage). Patient had the following side effects: liver function test abnormal, pyrexia. Cytoxan dosage: Last Dose Recieved On 31oct'06, Dose Reduced To 450mg/kg On 21nov'06.. During the same period patient was treated with ADRIAMYCIN PFS (Last Dose Recieved On 31oct'06. Dose Reduced To 45mg/m2 On 21nov'06.) (View Adriamycin Pfs Review and Adriamycin Pfs Label ), NEULASTA (Last Dose Recieved On 01nov'06.) (View Neulasta Review and Neulasta Label ), BEVACIZUMAB (Last Dose Recieved On 31oct'06.) (View Bevacizumab Review and Bevacizumab Label ), AMBIEN (View Ambien Review and Ambien Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), POTASSIUM CHLORIDE (1 Dosage Form=1 Tab.) (View Potassium Chloride Review and Potassium Chloride Label ), NAPROXEN (View Naproxen Review and Naproxen Label ), PREVACID (View Prevacid Review and Prevacid Label ). Patient was hospitalized.

5606107-5 | Multi-organ Failure, Progressive Multifocal Leukoencephalopathy
on Jan 25, 2008 Male patient from UNITED STATES , 69 years of age, was diagnosed with immunosuppression, vasculitis (What is vasculitis?), rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: multi-organ failure, progressive multifocal leukoencephalopathy. Cytoxan dosage: . During the same period patient was treated with REMICADE (Infliximab Recombinant Lyophilized Powder.) (View Remicade Review and Remicade Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ), COLCHICINE (View Colchicine Review and Colchicine Label ), FLECAINIDE ACETATE (View Flecainide Acetate Review and Flecainide Acetate Label ), HYTRIN (View Hytrin Review and Hytrin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ).

5602725-9 | Liver Function Test Abnormal, Pyrexia
Patient was taking Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: liver function test abnormal, pyrexia on Jan 24, 2008 from UNITED STATES Additional patient health information: Female patient , 61 years of age, weighting 123.5 lb, was diagnosed with breast cancer (What is breast cancer?), colony stimulating factor prophylaxis, insomnia, hypertension, mineral supplementation, arthralgia, peptic ulcer (What is peptic ulcer?) and. Cytoxan dosage: Last Dose Recieved On 31oct'06, Dose Reduced To 450mg/kg On 21nov'06.. During the same period patient was treated with ADRIAMYCIN PFS (Last Dose Recieved On 31oct'06. Dose Reduced To 45mg/m2 On 21nov'06.) (View Adriamycin Pfs Review and Adriamycin Pfs Label ), NEULASTA (Last Dose Recieved On 01nov'06.) (View Neulasta Review and Neulasta Label ), BEVACIZUMAB (Last Dose Recieved On 31oct'06.) (View Bevacizumab Review and Bevacizumab Label ), AMBIEN (View Ambien Review and Ambien Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), POTASSIUM CHLORIDE (1 Dosage Form=1 Tab.) (View Potassium Chloride Review and Potassium Chloride Label ), NAPROXEN (View Naproxen Review and Naproxen Label ), PREVACID (View Prevacid Review and Prevacid Label ). Patient was hospitalized.

5582704-0 | Clostridium Difficile Colitis, Fatigue, Febrile Neutropenia, Nausea, Oedema Peripheral, Pancytopenia
Adverse event was reported on Dec 27, 2007 by a Female patient taking Cytoxan (View Usage) (Dosage: ) was diagnosed with neoplasm malignant, anaemia of malignant disease, blood magnesium decreased and. Location: UNITED STATES , 59 years of age, weighting 119.0 lb, Patient had the following side effects: clostridium difficile colitis, fatigue, febrile neutropenia, nausea (What is nausea?), oedema peripheral, pancytopenia. During the same period patient was treated with TAXOTERE (View Taxotere Review and Taxotere Label ), EPIRUBICIN (View Epirubicin Review and Epirubicin Label ), EPOGEN (View Epogen Review and Epogen Label ), BENADRYL (11-oct-07, 15-oct-07, 19-oct-07, 22-oct-07 (12.5mg, 1 In 1 Day) And Interrupted Inbetween) (View Benadryl Review and Benadryl Label ), MIRACLE MOUTHWASH (View Miracle Mouthwash Review and Miracle Mouthwash Label ), MYLANTA (View Mylanta Review and Mylanta Label ), HYDROCODONE BITARTRATE (View Hydrocodone Bitartrate Review and Hydrocodone Bitartrate Label ), IBUPROFEN (View Ibuprofen Review and Ibuprofen Label ). Patient was hospitalized and became disabled.

5537079-X | Asthenia, Cerebrovascular Accident, Confusional State, Mental Status Changes, Multi-organ Failure, Progressive Multifocal Leukoencephalopathy, Respiratory Distress
on Dec 05, 2007 Male patient from UNITED STATES , 69 years of age, was diagnosed with vasculitis (What is vasculitis?), rheumatoid arthritis (What is rheumatoid arthritis?) and was treated with Cytoxan (View Usage). After Cytoxan was administered, patient had the following side effects: asthenia, cerebrovascular accident, confusional state, mental status changes, multi-organ failure, progressive multifocal leukoencephalopathy, respiratory distress. Cytoxan dosage: . During the same period patient was treated with REMICADE (Infliximab Recombinant Lyophilized Powder.) (View Remicade Review and Remicade Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), COLCHICINE (View Colchicine Review and Colchicine Label ).

5528820-0 | Febrile Neutropenia, Hypotension, Pneumonia
on Nov 20, 2007 Female patient from UNITED STATES , 49 years of age, weighting 103.6 lb, was diagnosed with breast cancer (What is breast cancer?) and was treated with Cytoxan (View Usage). Patient experienced the following unwanted or unexpected effects: febrile neutropenia, hypotension, pneumonia (What is pneumonia?). Cytoxan dosage: . During the same period patient was treated with ADRIAMYCIN PFS (View Adriamycin Pfs Review and Adriamycin Pfs Label ), TAXOTERE (View Taxotere Review and Taxotere Label ), NEULASTA (View Neulasta Review and Neulasta Label ). Patient was hospitalized.

5527497-8 | Abdominal Pain, Caecitis, Colitis, Hypertension, Hypotension, Neutropenia, Sepsis, Thrombocytopenia
Patient was taking Cytoxan (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), caecitis, colitis, hypertension, hypotension, neutropenia, sepsis (What is sepsis?), thrombocytopenia on Nov 16, 2007 from UNITED STATES Additional patient health information: Female patient , 73 years of age, weighting 138.9 lb, was diagnosed with breast cancer (What is breast cancer?) and. Cytoxan dosage: . During the same period patient was treated with ADRIAMYCIN (View Adriamycin Review and Adriamycin Label ), TAXOTERE (View Taxotere Review and Taxotere Label ), NEULASTA (View Neulasta Review and Neulasta 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 Cytoxan 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 Cytoxan quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Cytoxan 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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Cytoxan Reactions
Abdominal PainWhat is Abdominal pain?
Anaemia
Asthenia
Cardiac Failure Congestive
Cough
Death
Dehydration
Diarrhoea
Dyspnoea
Erythema
Fatigue
Febrile Neutropenia
Haemoglobin Decreased
HeadacheWhat is Headache?
Hypertension
Hypotension
Intestinal Perforation
Malignant Neoplasm Progression
Mucosal Inflammation
NauseaWhat is Nausea?
Neutropenia
Pancytopenia
Platelet Count Decreased
PneumoniaWhat is Pneumonia?
Pyrexia
RashWhat is Rash?
SepsisWhat is Sepsis?
Thrombocytopenia
Vomiting
White Blood Cell Count Decreased
Cytoxan 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 Cytoxan 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!