PROTOPIC Side Effects

7020728-7 | Skin Papilloma
on Sep 16, 2010 Male patient from FRANCE , 25 years of age, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: skin papilloma. Protopic dosage: 0.1%, Bid, Topical. During the same period patient was treated with DEXERYL (WHITE SOFT PARAFFIN, PARAFFIN, LIQUID) (View Dexeryl (white Soft Paraffin, Paraffin, Liquid) Review and Dexeryl (white Soft Paraffin, Paraffin, Liquid) Label ).

7018597-4 | Benign Vulval Neoplasm, Genital Herpes, Off Label Use, Squamous Cell Carcinoma
Patient was taking Protopic (View Usage). Patient had the following side effects: benign vulval neoplasm, genital herpes, off label use, squamous cell carcinoma on Sep 13, 2010 from GERMANY Additional patient health information: Female patient , 44 years of age, was diagnosed with benign familial pemphigus and. Protopic dosage: 0.1 %, Uid/qd, Topical.

7004987-2 | Metastases To Lymph Nodes
Adverse event was reported on Sep 08, 2010 by a Female patient taking Protopic (View Usage) (Dosage: Topical) was diagnosed with oral lichen planus and. Location: JAPAN , 80 years of age, After Protopic was administered, patient had the following side effects: metastases to lymph nodes. During the same period patient was treated with STEROID OINTMENT (View Steroid Ointment Review and Steroid Ointment Label ).

6988356-7 | Prostatic Specific Antigen Increased
on Sep 03, 2010 Male patient from UNITED STATES , 84 years of age, weighting 160.9 lb, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: prostatic specific antigen increased. Protopic dosage: 0.1 %, Bid, Topical.


6986135-8 | Myeloid Leukaemia
on Sep 02, 2010 Female patient from BELGIUM , 96 years of age, weighting 110.2 lb, was diagnosed with eczema (What is eczema?) and was treated with Protopic (View Usage). Patient had the following side effects: myeloid leukaemia. Protopic dosage: . During the same period patient was treated with COVERSYL PLUS (INAPAMIDE, PERINDOPRIL ERUMINE) (View Coversyl Plus (inapamide, Perindopril Erumine) Review and Coversyl Plus (inapamide, Perindopril Erumine) Label ), TEMESTA (ASTEMIZOLE) (View Temesta (astemizole) Review and Temesta (astemizole) Label ).

6979893-X | Asthenia, Disability, Eczema, Food Intolerance, Hepatitis Toxic, Nausea
Patient was taking Protopic (View Usage). After Protopic was administered, patient had the following side effects: asthenia, disability, eczema (What is eczema?), food intolerance, hepatitis toxic, nausea (What is nausea?) on Aug 30, 2010 from FRANCE Additional patient health information: Female patient , 66 years of age, weighting 112.4 lb, was diagnosed with dermatitis atopic and. Protopic dosage: 0.1 %, Bid, Topical. During the same period patient was treated with DIVINA (MEDROXYPROGESTERONE ACETATE) (View Divina (medroxyprogesterone Acetate) Review and Divina (medroxyprogesterone Acetate) Label ).

6967565-7 | Myeloid Leukaemia
Adverse event was reported on Aug 16, 2010 by a Female patient taking Protopic (View Usage) (Dosage: 1 %, /d) was diagnosed with eczema (What is eczema?) and. Location: BELGIUM , 96 years of age, weighting 110.2 lb, Patient experienced the following unwanted or unexpected effects: myeloid leukaemia. During the same period patient was treated with COVERSYL PLUS (INDAPAMIDE, PERINDOPRIL ERBUMINE) (View Coversyl Plus (indapamide, Perindopril Erbumine) Review and Coversyl Plus (indapamide, Perindopril Erbumine) Label ), TEMESTA (ASTEMIZOLE) (View Temesta (astemizole) Review and Temesta (astemizole) Label ).

6964072-2 | Dermatitis Atopic, Lung Disorder, Off Label Use, Prurigo, Vitiligo
on Aug 20, 2010 Male patient from FRANCE , 86 years of age, was diagnosed with dermatitis atopic, eczema (What is eczema?), vitiligo and was treated with Protopic (View Usage). Patient had the following side effects: dermatitis atopic, lung disorder, off label use, prurigo, vitiligo. Protopic dosage: 0.1%, Bid, Topical. Patient was hospitalized.

6956010-3 | Disease Recurrence, Eczema, Hepatitis
on Aug 11, 2010 Female patient from FRANCE , 66 years of age, weighting 112.4 lb, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). After Protopic was administered, patient had the following side effects: disease recurrence, eczema (What is eczema?), hepatitis (What is hepatitis?). Protopic dosage: 0.1 %, Bid, Topical. During the same period patient was treated with MEDROXYPROGESTERONE ACETATE (View Medroxyprogesterone Acetate Review and Medroxyprogesterone Acetate Label ).

6914377-6 | Depression, Economic Problem, Hyperphagia, Off Label Use
Patient was taking Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: depression (What is depression?), economic problem, hyperphagia, off label use on Jul 23, 2010 from BRAZIL Additional patient health information: Female patient , 16 years of age, weighting 97.00 lb, was diagnosed with vitiligo and. Protopic dosage: 0.1 %, Topical. During the same period patient was treated with EPISOL (View Episol Review and Episol Label ).

6902533-2 | Lung Disorder, Off Label Use
Adverse event was reported on Jul 20, 2010 by a Male patient taking Protopic (View Usage) (Dosage: 0.1 %, Bid, Topical; 0.1 %, Bid, Topical; 0.1 %, Bid, Topical) was diagnosed with dermatitis atopic, eczema (What is eczema?), prurigo and. Location: FRANCE , 86 years of age, Patient had the following side effects: lung disorder, off label use. Patient was hospitalized.

6865988-8 | Hepatic Function Abnormal, Lymphadenopathy Mediastinal, Metastases To Bone Marrow, Metastases To Liver, Metastases To Lung, Metastases To Lymph Nodes, Respiratory Failure, Squamous Cell Carcinoma
on Jul 12, 2010 Male patient from JAPAN , 60 years of age, was diagnosed with lichen planus and was treated with Protopic (View Usage). After Protopic was administered, patient had the following side effects: hepatic function abnormal, lymphadenopathy mediastinal, metastases to bone marrow, metastases to liver, metastases to lung, metastases to lymph nodes, respiratory failure, squamous cell carcinoma. Protopic dosage: 0.1%, Topical. During the same period patient was treated with RINDERON VG (GENTAMICIN SULFATE, BETAMETHASONE VALERATE) (View Rinderon-vg (gentamicin Sulfate, Betamethasone Valerate) Review and Rinderon-vg (gentamicin Sulfate, Betamethasone Valerate) Label ). Patient was hospitalized and became disabled.

6839691-4 | Aspartate Aminotransferase Increased, Haematocrit Decreased, Haemoglobin Decreased, Laboratory Test Abnormal, Metastases To Bone, Metastases To Liver, Metastases To Lung, Metastases To Lymph Nodes, Red Blood Cell Count Decreased
on Jun 30, 2010 Male patient from JAPAN , 60 years of age, was diagnosed with lichen planus and was treated with Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: aspartate aminotransferase increased, haematocrit decreased, haemoglobin decreased, laboratory test abnormal, metastases to bone, metastases to liver, metastases to lung, metastases to lymph nodes, red blood cell count decreased. Protopic dosage: 0.1 %, Topical. During the same period patient was treated with RINDERON VG (GENTAMICIN SULFATE, BETAMETHASONE VALERATE) OINTMENT (View Rinderon-vg (gentamicin Sulfate, Betamethasone Valerate) Ointment Review and Rinderon-vg (gentamicin Sulfate, Betamethasone Valerate) Ointment Label ). Patient was hospitalized and became disabled.

6816603-0 | Lymphadenopathy, Nodule
Patient was taking Protopic (View Usage). Patient had the following side effects: lymphadenopathy, nodule on Jun 21, 2010 from NETHERLANDS Additional patient health information: Female patient , 76 years of age, weighting 187.4 lb, was diagnosed with dermatitis atopic and. Protopic dosage: 1 Df, /d, Cutaneous. During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), CUTIVATE (FLUTICASONE PROPIONATE) (View Cutivate (fluticasone Propionate) Review and Cutivate (fluticasone Propionate) Label ), NEORAL (View Neoral Review and Neoral Label ).

6809853-0 | Lung Disorder, Off Label Use
Adverse event was reported on Jun 15, 2010 by a Male patient taking Protopic (View Usage) (Dosage: 0.1 %, /d, Topical) was diagnosed with eczema (What is eczema?), prurigo and. Location: FRANCE , 86 years of age, After Protopic was administered, patient had the following side effects: lung disorder, off label use. Patient was hospitalized.

6785107-6 | Lung Disorder
on Jun 09, 2010 Male patient from FRANCE , 87 years of age, was treated with Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: lung disorder. Protopic dosage: .

6785015-0 | Cervix Carcinoma
on Jun 09, 2010 Female patient from FRANCE , 63 years of age, was treated with Protopic (View Usage). Patient had the following side effects: cervix carcinoma. Protopic dosage: Topical. During the same period patient was treated with MEDROL (Oral) (View Medrol Review and Medrol Label ), PLAQUENIL (Oral) (View Plaquenil Review and Plaquenil Label ), METHOTREXATE (Oral) (View Methotrexate Review and Methotrexate Label ), DISULONE (DAPSONE, FEEROUS OXALATE) (Oral) (View Disulone (dapsone, Feerous Oxalate) Review and Disulone (dapsone, Feerous Oxalate) Label ), REMICADE (Iv Nos) (View Remicade Review and Remicade Label ), THALIDOMIDE (Oral) (View Thalidomide Review and Thalidomide Label ), MINCOYCLINE (MINCOYCLINE) (Oral) (View Mincoycline (mincoycline) Review and Mincoycline (mincoycline) Label ). Patient was hospitalized.

6782785-2 | Confusional State, Coordination Abnormal, Depressed Level Of Consciousness, Hallucination, Hepatic Failure, Hypocalcaemia, Hypomagnesaemia
Patient was taking Protopic (View Usage). After Protopic was administered, patient had the following side effects: confusional state, coordination abnormal, depressed level of consciousness, hallucination, hepatic failure, hypocalcaemia, hypomagnesaemia on Jun 09, 2010 from NETHERLANDS Additional patient health information: Male patient , 45 years of age, weighting 119.0 lb, was diagnosed with dermatitis exfoliative and. Protopic dosage: Unk, Topical. During the same period patient was treated with SUBOXONE (Unk, Sublingual) (View Suboxone Review and Suboxone Label ), PENTASA (View Pentasa Review and Pentasa Label ), REFUSAL (DISULFIRAM) (View Refusal (disulfiram) Review and Refusal (disulfiram) Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), TEMAZEPAM (View Temazepam Review and Temazepam Label ), MOVICOLON (MACROGOL, POTASSIUM CHLORIDE, SODIUM BICARBONATE, SODIUM CH (View Movicolon (macrogol, Potassium Chloride, Sodium Bicarbonate, Sodium Ch Review and Movicolon (macrogol, Potassium Chloride, Sodium Bicarbonate, Sodium Ch Label ), PAROXETINE HCL (View Paroxetine Hcl Review and Paroxetine Hcl Label ), SELOKEEN (METOPROLOL SUCCINATE) (View Selokeen (metoprolol Succinate) Review and Selokeen (metoprolol Succinate) Label ). Patient was hospitalized.

6776440-2 | Nodule
Adverse event was reported on Jun 07, 2010 by a Female patient taking Protopic (View Usage) (Dosage: 1 Df, Cutaneous) was diagnosed with dermatitis atopic and. Location: NETHERLANDS , 76 years of age, weighting 187.4 lb, Patient experienced the following unwanted or unexpected effects: nodule. During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), CUTIVATE (FLUTICASONE PROPIONATE) (View Cutivate (fluticasone Propionate) Review and Cutivate (fluticasone Propionate) Label ), NEORAL (View Neoral Review and Neoral Label ).

6730568-1 | Lymphadenopathy, Sarcoma
on May 03, 2010 Male patient from UNITED STATES , 65 years of age, was diagnosed with seborrhoeic dermatitis and was treated with Protopic (View Usage). Patient had the following side effects: lymphadenopathy, sarcoma. Protopic dosage: Topical.

6727713-0 | Hordeolum
on May 05, 2010 Female patient from SPAIN , 40 years of age, weighting 119.0 lb, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). After Protopic was administered, patient had the following side effects: hordeolum. Protopic dosage: Topical.

6719925-7 | Hypergammaglobulinaemia, Mycosis Fungoides, Pain
Patient was taking Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: hypergammaglobulinaemia, mycosis fungoides, pain (What is pain?) on Apr 29, 2010 from FRANCE Additional patient health information: Female patient , 36 years of age, . Protopic dosage: . During the same period patient was treated with DERMOVAL (CLOBETASOL PROPIONATE) (View Dermoval (clobetasol Propionate) Review and Dermoval (clobetasol Propionate) Label ).

6710473-7 | Metastases To Lung, Metastases To Lymph Nodes, Papilloma Viral Infection, Penile Malignant Neoplasm, Penis Carcinoma Metastatic
Adverse event was reported on Apr 26, 2010 by a Male patient taking Protopic (View Usage) (Dosage: %, /d, Topical) was diagnosed with balanitis and. Location: SPAIN , 59 years of age, Patient had the following side effects: metastases to lung, metastases to lymph nodes, papilloma viral infection, penile malignant neoplasm, penis carcinoma metastatic. Patient was hospitalized.

6709436-7 | B-cell Lymphoma
on Oct 03, 2006 Male patient from FINLAND , 54 years of age, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). After Protopic was administered, patient had the following side effects: b-cell lymphoma. Protopic dosage: 0.03%, Uid/qd/ Topical. During the same period patient was treated with PROSCAR (View Proscar Review and Proscar Label ). Patient was hospitalized.

6707930-6 | Hodgkin's Disease Stage I
on Jun 13, 2006 Female patient from FINLAND , 49 years of age, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: hodgkin's disease stage i. Protopic dosage: Df, Bid, Topical. During the same period patient was treated with ESTROGENS SOL/INJ (View Estrogens Sol/inj Review and Estrogens Sol/inj Label ).

6701214-8 | Application Site Oedema, Application Site Pain, Burning Sensation, Dermatitis Atopic, Off Label Use, Rebound Effect
Patient was taking Protopic (View Usage). Patient had the following side effects: application site oedema, application site pain, burning sensation, dermatitis atopic, off label use, rebound effect on Apr 16, 2010 from FRANCE Additional patient health information: Female patient , 37 years of age, was diagnosed with seborrhoeic dermatitis and. Protopic dosage: 1 Df, Uid/qd; Topical. During the same period patient was treated with INFLUENZA VACCINE (INFLUENZA VACCINE) (View Influenza Vaccine (influenza Vaccine) Review and Influenza Vaccine (influenza Vaccine) Label ), DESLORATADINE (View Desloratadine Review and Desloratadine Label ).

6700461-9 | Condition Aggravated, Neurodermatitis
Adverse event was reported on Apr 10, 2010 by a Female patient taking Protopic (View Usage) (Dosage: 2 G, Other, Topical) was diagnosed with neurodermatitis and. Location: GERMANY , 33 years of age, After Protopic was administered, patient had the following side effects: condition aggravated, neurodermatitis. During the same period patient was treated with PREDNISOLONE (View Prednisolone Review and Prednisolone Label ). Patient was hospitalized.

6659921-1 | Hodgkin's Disease
on Mar 16, 2010 Female patient from IRELAND , 24 years of age, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: hodgkin's disease (What is hodgkin's disease?). Protopic dosage: Topical. Patient was hospitalized.

6649809-4 | Malignant Melanoma
on Mar 17, 2010 Female patient from UNITED STATES , child 12 years of age, was diagnosed with skin lesion, vitiligo and was treated with Protopic (View Usage). Patient had the following side effects: malignant melanoma. Protopic dosage: 0.03%, Bid, Topical.

6649765-9 | Malignant Melanoma
Patient was taking Protopic (View Usage). After Protopic was administered, patient had the following side effects: malignant melanoma on Mar 17, 2010 from UNITED STATES Additional patient health information: Female patient , child 12 years of age, was diagnosed with vitiligo and. Protopic dosage: 0.1 %, Bid, Topical.

6642697-1 | Leukaemia
Adverse event was reported on Feb 24, 2010 by a Male patient taking Protopic (View Usage) (Dosage: ) . Location: BELGIUM , 56 years of age, Patient experienced the following unwanted or unexpected effects: leukaemia.

6634187-7 | Head And Neck Cancer, Squamous Cell Carcinoma
on Feb 22, 2010 Female patient from UNITED KINGDOM , 80 years of age, was diagnosed with eczema (What is eczema?) and was treated with Protopic (View Usage). Patient had the following side effects: head and neck cancer (What is head and neck cancer?), squamous cell carcinoma. Protopic dosage: 0.1%, Prn, Topical. During the same period patient was treated with FEXOFENADINE HCL (View Fexofenadine Hcl Review and Fexofenadine Hcl Label ), LIPOBASE (LOCOBASE) (View Lipobase (locobase) Review and Lipobase (locobase) Label ), BALNEUM PLUS (LAUROMACROGOL, GLYCINE MAX SEED OIL) (View Balneum Plus (lauromacrogol, Glycine Max Seed Oil) Review and Balneum Plus (lauromacrogol, Glycine Max Seed Oil) Label ).

6622762-5 | Alanine Aminotransferase Increased, Blood Cholesterol Abnormal, Gamma-glutamyltransferase Increased
on Feb 23, 2010 Female patient from BRAZIL , 31 years of age, weighting 147.7 lb, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). After Protopic was administered, patient had the following side effects: alanine aminotransferase increased, blood cholesterol abnormal, gamma-glutamyltransferase increased. Protopic dosage: 0.1 %, /d, Topical. During the same period patient was treated with EBASTEL (EBASTINE) (View Ebastel (ebastine) Review and Ebastel (ebastine) Label ).

6616181-5 | Alopecia Totalis, Lymphadenopathy
Patient was taking Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: alopecia totalis, lymphadenopathy on Feb 03, 2010 from ITALY Additional patient health information: Female patient , 14 years of age, was diagnosed with dermatitis allergic and. Protopic dosage: .

6613102-6 | Pruritus, T-cell Lymphoma
Adverse event was reported on Feb 03, 2010 by a Female patient taking Protopic (View Usage) (Dosage: ) was diagnosed with dermatitis atopic and. Location: ITALY , 30 years of age, Patient had the following side effects: pruritus, t-cell lymphoma.

6609218-0 |
on Feb 18, 2010 Female patient from UNITED STATES , 49 years of age, was diagnosed with dermatitis contact and was treated with Protopic (View Usage). . Protopic dosage: 0.1%, Bid, Topical.

6600326-7 | Burns Second Degree, Skin Burning Sensation
on Feb 11, 2010 Female patient from SOUTH AFRICA , 57 years of age, weighting 198.4 lb, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: burns second degree, skin burning sensation. Protopic dosage: Topical. During the same period patient was treated with SERETIDE (FLUITICASONE PROPIONATE) (View Seretide (fluiticasone Propionate) Review and Seretide (fluiticasone Propionate) Label ), SINGULAIR (View Singulair Review and Singulair Label ), PREMARIN (View Premarin Review and Premarin Label ), TOPZOL (TIOCONAZOLE) (View Topzol (tioconazole) Review and Topzol (tioconazole) Label ), PURICOS (ALLOPURINOL) (View Puricos (allopurinol) Review and Puricos (allopurinol) Label ).

6598045-9 | Neurilemmoma
Patient was taking Protopic (View Usage). Patient had the following side effects: neurilemmoma on Feb 04, 2010 from BRAZIL Additional patient health information: Female patient , 26 years of age, was diagnosed with seborrhoeic dermatitis, acne (What is acne?) and. Protopic dosage: Topical. During the same period patient was treated with ISOTRETINOIN (20 Mg, Uid/qd, Oral) (View Isotretinoin Review and Isotretinoin Label ). Patient was hospitalized.

6593996-3 | Burns Second Degree, Skin Burning Sensation
Adverse event was reported on Feb 01, 2010 by a Female patient taking Protopic (View Usage) (Dosage: Topical) was diagnosed with dermatitis atopic and. Location: SOUTH AFRICA , 57 years of age, weighting 198.4 lb, After Protopic was administered, patient had the following side effects: burns second degree, skin burning sensation.

6578668-3 | Angiomyolipoma
on Jan 25, 2010 Female patient from UNITED STATES , 72 years of age, was diagnosed with vitiligo and was treated with Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: angiomyolipoma. Protopic dosage: Topical.

6552941-7 | Application Site Inflammation, Application Site Reaction, Burning Sensation
on Jan 08, 2010 Female patient from SPAIN , 46 years of age, weighting 121.3 lb, was treated with Protopic (View Usage). Patient had the following side effects: application site inflammation, application site reaction, burning sensation. Protopic dosage: Topical. During the same period patient was treated with EUTIROX (LEVOTHYROXINE) (View Eutirox (levothyroxine) Review and Eutirox (levothyroxine) Label ).

6544583-4 | Condition Aggravated, Dyspnoea, Laryngeal Oedema, Rash Macular
Patient was taking Protopic (View Usage). After Protopic was administered, patient had the following side effects: condition aggravated, dyspnoea, laryngeal oedema, rash macular on Jan 06, 2010 from BRAZIL Additional patient health information: Female patient , 77 years of age, weighting 141.1 lb, was diagnosed with skin irritation and. Protopic dosage: 0.1%, Topical. During the same period patient was treated with RITMONORM (PROPAFENONE HYDROCHLORIDE) (View Ritmonorm (propafenone Hydrochloride) Review and Ritmonorm (propafenone Hydrochloride) Label ), ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE (View Enalapril Maleate And Hydrochlorothiazide Review and Enalapril Maleate And Hydrochlorothiazide Label ), LASIX (View Lasix Review and Lasix Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), DOMPERIDONE (DOMPERIDONE) (View Domperidone (domperidone) Review and Domperidone (domperidone) Label ), BROMAZEPAM (BROMAZEPAM) (View Bromazepam (bromazepam) Review and Bromazepam (bromazepam) Label ), PARACIL (PARACETAMOL) (View Paracil (paracetamol) Review and Paracil (paracetamol) Label ), B COMPLEX (VITAMIN B KOMPLEX STANDARD) TABLET ONGOING (View B Complex (vitamin-b-komplex Standard) Tablet Ongoing Review and B Complex (vitamin-b-komplex Standard) Tablet Ongoing Label ).

6542813-6 | Alanine Aminotransferase Increased, Blood Cholesterol Abnormal, Gamma-glutamyltransferase Increased
Adverse event was reported on Jan 05, 2010 by a Female patient taking Protopic (View Usage) (Dosage: 0.1%, D, Topical) was diagnosed with dermatitis atopic and. Location: BRAZIL , 31 years of age, weighting 147.7 lb, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, blood cholesterol abnormal, gamma-glutamyltransferase increased. During the same period patient was treated with EBASTEL (EBASTINE) (View Ebastel (ebastine) Review and Ebastel (ebastine) Label ).

6536675-0 | Dyspnoea, Laryngeal Oedema, Rash Macular
on Dec 28, 2009 Female patient from BRAZIL , 77 years of age, weighting 141.1 lb, was diagnosed with skin irritation and was treated with Protopic (View Usage). Patient had the following side effects: dyspnoea, laryngeal oedema, rash macular. Protopic dosage: 0.1%, Topical. During the same period patient was treated with RITMONORM (PROPAFENONE HYDROCHLORIDE) (View Ritmonorm (propafenone Hydrochloride) Review and Ritmonorm (propafenone Hydrochloride) Label ), ENALAPRIL MALEATE AND HYDROCHLOROTHIAZIDE (View Enalapril Maleate And Hydrochlorothiazide Review and Enalapril Maleate And Hydrochlorothiazide Label ), LASIX (View Lasix Review and Lasix Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), DOMPERIDONE (DOMEPERIDONE) (View Domperidone (domeperidone) Review and Domperidone (domeperidone) Label ), TICLID (View Ticlid Review and Ticlid Label ), FLUOXETINE (View Fluoxetine Review and Fluoxetine Label ), BROMAZEPAM (BROMAZEPAM) (View Bromazepam (bromazepam) Review and Bromazepam (bromazepam) Label ).

6527366-0 | Actinic Keratosis
on Dec 17, 2009 Male patient from GERMANY , 43 years of age, weighting 185.2 lb, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). After Protopic was administered, patient had the following side effects: actinic keratosis. Protopic dosage: .

6526438-4 | Breast Cancer Stage Ii, Hodgkin's Disease Nodular Sclerosis Stage Ii Supradiaphragmatic
Patient was taking Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: breast cancer stage ii, hodgkin's disease nodular sclerosis stage ii supradiaphragmatic on Dec 17, 2009 from UNITED STATES Additional patient health information: Female patient , 41 years of age, weighting 244.7 lb, . Protopic dosage: 0.1%, D. During the same period patient was treated with ELIDEL (1 % D) (View Elidel Review and Elidel Label ).

6525986-0 | Herpes Zoster, Impetigo, Kaposi's Varicelliform Eruption, Skin Papilloma
Adverse event was reported on Dec 14, 2009 by a Female patient taking Protopic (View Usage) (Dosage: 0.03 %, Topical) was diagnosed with dermatitis atopic and. Location: JAPAN , child 3 years of age, Patient had the following side effects: herpes zoster, impetigo (What is impetigo?), kaposi's varicelliform eruption, skin papilloma. During the same period patient was treated with HIRUDOID (HEPARINOID) LOTION (View Hirudoid (heparinoid) Lotion Review and Hirudoid (heparinoid) Lotion Label ), LIDOMEX (PREDNISOLONE VALEROACETATE) LOTION (View Lidomex (prednisolone Valeroacetate) Lotion Review and Lidomex (prednisolone Valeroacetate) Lotion Label ), PALDES (CLOBETASONE BUTYRATE) LOTION (View Paldes (clobetasone Butyrate) Lotion Review and Paldes (clobetasone Butyrate) Lotion Label ), WHITE PETROLEUM (PETROLATUM) FORMULATION (View White Petroleum (petrolatum) Formulation Review and White Petroleum (petrolatum) Formulation Label ), PALDES (CLOBETASONE BUTYRATE) OINTMENT (View Paldes (clobetasone Butyrate) Ointment Review and Paldes (clobetasone Butyrate) Ointment Label ), ALLOMIDON (DEPRODONE PROPIONATE) OINTMENT (View Allomidon (deprodone Propionate) Ointment Review and Allomidon (deprodone Propionate) Ointment Label ), LIDOMEX (PREDNISOLONE VALEROACETATE) OINTMENT (View Lidomex (prednisolone Valeroacetate) Ointment Review and Lidomex (prednisolone Valeroacetate) Ointment Label ).

6506786-4 | Lymphopenia, Oral Candidiasis
on Dec 07, 2009 Male patient from UNITED STATES , 18 years of age, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). After Protopic was administered, patient had the following side effects: lymphopenia, oral candidiasis. Protopic dosage: 0.1 %, Topical.

6496765-8 | Alanine Aminotransferase Increased, Blood Cholesterol Abnormal, Gamma-glutamyltransferase Increased
on Dec 02, 2009 Female patient from BRAZIL , 31 years of age, weighting 147.7 lb, was diagnosed with dermatitis atopic and was treated with Protopic (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, blood cholesterol abnormal, gamma-glutamyltransferase increased. Protopic dosage: Topical.

6492857-8 | Acute Pulmonary Histoplasmosis, Testicular Microlithiasis, Testis Cancer
Patient was taking Protopic (View Usage). Patient had the following side effects: acute pulmonary histoplasmosis, testicular microlithiasis, testis cancer on Dec 01, 2009 from UNITED STATES Additional patient health information: Male patient , 18 years of age, weighting 125.0 lb, was diagnosed with vitiligo, eczema (What is eczema?) and. Protopic dosage: 0.1 %, D, Topical. During the same period patient was treated with ELIDEL (1%, D, Topical) (View Elidel Review and Elidel Label ), ZODERM (BENZOYL PEROXIDE) (View Zoderm (benzoyl Peroxide) Review and Zoderm (benzoyl Peroxide) Label ), CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label ).