ANDRODERM Side Effects

6932848-3 | Chromaturia, Meniscus Lesion, Urine Odour Abnormal
on Aug 06, 2010 Male patient from UNITED STATES , 40 years of age, weighting 274.9 lb, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: chromaturia, meniscus lesion, urine odour abnormal. Androderm dosage: 1 Patch, Q24h. Patient was hospitalized.

6909499-X | Angiofibroma, Condition Aggravated
Patient was taking Androderm (View Usage). Patient had the following side effects: angiofibroma, condition aggravated on Jul 26, 2010 from UNITED STATES Additional patient health information: Male patient , 36 years of age, was diagnosed with blood testosterone decreased and. Androderm dosage: Unk.

6855969-2 | Confusional State, Nausea, Vertigo
Adverse event was reported on Jul 16, 2010 by a Male patient taking Androderm (View Usage) (Dosage: 5.0 Mg 24 Hr Patch) was diagnosed with blood testosterone decreased and. Location: UNITED STATES , weighting 265.0 lb, After Androderm was administered, patient had the following side effects: confusional state, nausea (What is nausea?), vertigo.

6766938-5 | Aggression, Sexually Inappropriate Behaviour
on Jun 01, 2010 Male patient from UNITED STATES , 31 years of age, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: aggression, sexually inappropriate behaviour. Androderm dosage: 1 Patch, Daily. Patient was hospitalized.


6713103-3 | Blood Testosterone Decreased
on Jan 22, 2010 Male patient from UNITED STATES , 66 years of age, was diagnosed with depression (What is depression?), hypertension and was treated with Androderm (View Usage). Patient had the following side effects: blood testosterone decreased. Androderm dosage: 2.5mg Per Day. During the same period patient was treated with AMOXICILLIN (2cap Twice Per Day) (View Amoxicillin Review and Amoxicillin Label ), FLUOXETINE (10mg Per Day) (View Fluoxetine Review and Fluoxetine Label ), LISINOPRIL (20mg Per Day) (View Lisinopril Review and Lisinopril Label ).

6699844-5 | Rash
Patient was taking Androderm (View Usage). After Androderm was administered, patient had the following side effects: rash (What is rash?) on Apr 27, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 223.0 lb, . Androderm dosage: 5 Mg/24 Hr. Daily Transdermal.

6687485-5 | Product Quality Issue, Therapeutic Response Decreased
Adverse event was reported on Apr 16, 2010 by a Male patient taking Androderm (View Usage) (Dosage: 5 Mg/da Each Day Skin) was diagnosed with blood testosterone decreased and. Location: UNITED STATES , weighting 195.0 lb, Patient experienced the following unwanted or unexpected effects: product quality issue, therapeutic response decreased.

6555157-3 | Erythema
on Jan 26, 2010 Male patient from UNITED STATES , weighting 180.0 lb, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). Patient had the following side effects: erythema. Androderm dosage: 2.5 Mg Daily Patch. During the same period patient was treated with SAME (2.5 Mg Daily Patch) (View Same Review and Same Label ).

6543831-4 | Product Quality Issue
on Jan 19, 2010 Male patient from UNITED STATES , 73 years of age, weighting 280.0 lb, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). After Androderm was administered, patient had the following side effects: product quality issue. Androderm dosage: 5 Mg Day.

6524160-1 | Hot Flush, Night Sweats, Small Intestinal Obstruction
Patient was taking Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: hot flush, night sweats, small intestinal obstruction on Dec 21, 2009 from UNITED STATES Additional patient health information: Male patient , 71 years of age, was diagnosed with blood testosterone decreased and. Androderm dosage: 2.5 Mg, Daily. Patient was hospitalized.

6454750-6 | Accidental Exposure, Acne, Blood Testosterone Increased, Bone Development Abnormal, Cafe Au Lait Spots, Ear Infection, Growth Retardation, Hair Growth Abnormal, Increased Appetite
Adverse event was reported on Nov 18, 2009 by a Male patient taking Androderm (View Usage) (Dosage: 1 Patch, Daily) was diagnosed with blood testosterone decreased and. Location: UNITED STATES , weighting 115.1 lb, Patient had the following side effects: accidental exposure, acne (What is acne?), blood testosterone increased, bone development abnormal, cafe au lait spots, ear infection (What is ear infection?), growth retardation, hair growth abnormal, increased appetite. During the same period patient was treated with ANDROGEL (1 Application, Daily) (View Androgel Review and Androgel Label ), SINGULAIR (Unk) (View Singulair Review and Singulair Label ), ALLEGRA (Unk) (View Allegra Review and Allegra Label ).

6454749-X | Accidental Exposure, Acne, Blood Thyroid Stimulating Hormone Increased, Body Height Increased, Bone Development Abnormal, Growth Retardation, Hair Growth Abnormal, Hypertrichosis, Precocious Puberty
on Nov 18, 2009 Female patient from UNITED STATES , weighting 58.86 lb, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). After Androderm was administered, patient had the following side effects: accidental exposure, acne (What is acne?), blood thyroid stimulating hormone increased, body height increased, bone development abnormal, growth retardation, hair growth abnormal, hypertrichosis, precocious puberty. Androderm dosage: 1 Patch, Daily. During the same period patient was treated with ANDROGEL (1 Application, Daily) (View Androgel Review and Androgel Label ).

6384707-5 | Blood Testosterone Decreased, Blood Testosterone Free Decreased, Thyroid Cancer, Thyroid Disorder
on Sep 18, 2009 Male patient from UNITED STATES , weighting 295.9 lb, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: blood testosterone decreased, blood testosterone free decreased, thyroid cancer (What is thyroid cancer?), thyroid disorder. Androderm dosage: Apply 1 Patch, Daily.

6366799-2 | Haemorrhage, Lung Cyst
Patient was taking Androderm (View Usage). Patient had the following side effects: haemorrhage, lung cyst on Sep 11, 2009 from CANADA Additional patient health information: Male patient , 29 years of age, . Androderm dosage: Unk.

6357159-9 | Accidental Exposure, Acne, Blood Testosterone Increased, Bone Development Abnormal, Cafe Au Lait Spots, Ear Infection, Growth Retardation, Hair Growth Abnormal, Increased Appetite
Adverse event was reported on Sep 03, 2009 by a Male patient taking Androderm (View Usage) (Dosage: 1 Patch, Daily) was diagnosed with blood testosterone decreased and. Location: UNITED STATES , weighting 115.1 lb, After Androderm was administered, patient had the following side effects: accidental exposure, acne (What is acne?), blood testosterone increased, bone development abnormal, cafe au lait spots, ear infection (What is ear infection?), growth retardation, hair growth abnormal, increased appetite. During the same period patient was treated with ANDROGEL (1 Application, Daily) (View Androgel Review and Androgel Label ), SINGULAIR (Unk) (View Singulair Review and Singulair Label ), ALLEGRA (Unk) (View Allegra Review and Allegra Label ).

6357158-7 | Accidental Exposure, Body Height Increased, Bone Development Abnormal, Hair Growth Abnormal, Hypertrichosis, Precocious Puberty
on Sep 03, 2009 Female patient from UNITED STATES , weighting 58.86 lb, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: accidental exposure, body height increased, bone development abnormal, hair growth abnormal, hypertrichosis, precocious puberty. Androderm dosage: 1 Patch, Daily. During the same period patient was treated with ANDROGEL (1 Application, Daily) (View Androgel Review and Androgel Label ).

6336638-4 | Application Site Erythema, Application Site Irritation, Application Site Rash, Application Site Swelling, Discomfort
on Aug 31, 2009 Male patient from UNITED STATES , 48 years of age, weighting 195.0 lb, was diagnosed with blood testosterone decreased, nonspecific reaction and was treated with Androderm (View Usage). Patient had the following side effects: application site erythema, application site irritation, application site rash, application site swelling, discomfort. Androderm dosage: 1 Patch Once Daily Transdermal. During the same period patient was treated with ANDROGEL (4 Pumps Once Daily Top) (View Androgel Review and Androgel Label ).

6233792-X | Device Adhesion Issue
Patient was taking Androderm (View Usage). After Androderm was administered, patient had the following side effects: device adhesion issue on Jun 12, 2009 from UNITED STATES Additional patient health information: Male patient , 71 years of age, weighting 185.4 lb, was diagnosed with blood testosterone decreased and. Androderm dosage: 5 Mg Qd Transdermal Has Use At Least Since 12/0.

6173921-X | Application Site Irritation, Application Site Rash, Application Site Vesicles
Adverse event was reported on Apr 29, 2009 by a Male patient taking Androderm (View Usage) (Dosage: 5mg/day Daily Transdermal) . Location: UNITED STATES , weighting 190.0 lb, Patient experienced the following unwanted or unexpected effects: application site irritation, application site rash, application site vesicles.

6161860-X | Pain
on Apr 20, 2009 Male patient from UNITED STATES , 52 years of age, was diagnosed with hypogonadism, rheumatoid arthritis (What is rheumatoid arthritis?), depression (What is depression?), hypertension and was treated with Androderm (View Usage). Patient had the following side effects: pain (What is pain?). Androderm dosage: 5mg Per Day. During the same period patient was treated with OPANA (OXYMORPHONE HCL) (30mg Twice Per Day) (View Opana (oxymorphone Hcl) Review and Opana (oxymorphone Hcl) Label ), FLUOXETINE (40mg Per Day) (View Fluoxetine Review and Fluoxetine Label ), LISINOPRIL (1tab Per Day) (View Lisinopril Review and Lisinopril Label ), NABUMETONE (750mg Twice Per Day) (View Nabumetone Review and Nabumetone Label ), LORATADINE (10mg Per Day) (View Loratadine Review and Loratadine Label ), FOLIC ACID (1mg Per Day) (View Folic Acid Review and Folic Acid Label ).

6157589-4 | Pain
on Apr 10, 2009 Male patient from UNITED STATES , weighting 303.0 lb, was diagnosed with hypogonadism male, rheumatoid arthritis (What is rheumatoid arthritis?), myalgia, depression (What is depression?), hypertension, rhinitis allergic and was treated with Androderm (View Usage). After Androderm was administered, patient had the following side effects: pain (What is pain?). Androderm dosage: 5 Mg, 1 Patch, Daily. During the same period patient was treated with OPANA ER (30 Mg, Q12h) (View Opana Er Review and Opana Er Label ), FLUOXETINE (40 Mg, 1 Daily) (View Fluoxetine Review and Fluoxetine Label ), LISINOPRIL AND HYDROCHLOROTHIAZIDE (20 Mg/12.5 Mg, 1 Tab Daily) (View Lisinopril And Hydrochlorothiazide Review and Lisinopril And Hydrochlorothiazide Label ), NABUMETONE (750 Mg, 1 Tab Bid) (View Nabumetone Review and Nabumetone Label ), LORATADINE (10 Mg, 1 Tab, Daily) (View Loratadine Review and Loratadine Label ), FOLIC ACID (1 Mg, 1 Daily) (View Folic Acid Review and Folic Acid Label ).

6128206-4 | Hypersensitivity, Inflammation, Product Quality Issue
Patient was taking Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: hypersensitivity, inflammation, product quality issue on Mar 20, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 183.0 lb, was diagnosed with blood testosterone decreased and. Androderm dosage: 5mg/day Patch Qd Transdermal.

6100146-6 | Blood Testosterone Decreased, Product Quality Issue
Adverse event was reported on Mar 02, 2009 by a Male patient taking Androderm (View Usage) (Dosage: 5 Daily Transdermal About 9 Or 10 Years) was diagnosed with hypogonadism and. Location: UNITED STATES , weighting 205.0 lb, Patient had the following side effects: blood testosterone decreased, product quality issue.

6045564-X | Application Site Erythema, Application Site Induration, Application Site Irritation, Back Pain, Bone Neoplasm, Hepatic Function Abnormal, Psoriasis, Renal Impairment
on Jan 08, 2009 Male patient from UNITED STATES , 56 years of age, was diagnosed with hypogonadism male, diabetes mellitus, pain in extremity, glaucoma (What is glaucoma?), blood cholesterol increased, hypertension and was treated with Androderm (View Usage). After Androderm was administered, patient had the following side effects: application site erythema, application site induration, application site irritation, back pain (What is back pain?), bone neoplasm, hepatic function abnormal, psoriasis, renal impairment. Androderm dosage: 5 Mg, Daily. During the same period patient was treated with METFORMIN (Unk) (View Metformin Review and Metformin Label ), GLYBURIDE (Unk) (View Glyburide Review and Glyburide Label ), GABAPENTIN (Unk) (View Gabapentin Review and Gabapentin Label ), GLAUCOMA EYEDROPS (Unk) (View Glaucoma Eyedrops Review and Glaucoma Eyedrops Label ), LIPITOR (Unk) (View Lipitor Review and Lipitor Label ), DIOVAN /01319601/ (Unk) (View Diovan /01319601/ Review and Diovan /01319601/ Label ), AMLODIPINE (Unk) (View Amlodipine Review and Amlodipine Label ).

6014093-1 | Anorgasmia
on Nov 26, 2007 Male patient from UNITED STATES , 70 years of age, was treated with Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: anorgasmia. Androderm dosage: 2.5mg Per Day. During the same period patient was treated with AVODART (.5mg Per Day) (View Avodart Review and Avodart Label ).

5928508-8 | Application Site Erythema, Application Site Pruritus, Application Site Swelling, Application Site Vesicles, Idiopathic Thrombocytopenic Purpura
Patient was taking Androderm (View Usage). Patient had the following side effects: application site erythema, application site pruritus, application site swelling, application site vesicles, idiopathic thrombocytopenic purpura on Oct 13, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 229.3 lb, was diagnosed with blood testosterone decreased, cardiovascular disorder, glaucoma (What is glaucoma?), blood cholesterol, gastrooesophageal reflux disease and. Androderm dosage: 1 Patch, Daily. During the same period patient was treated with ANDROGEL (10 G, Daily) (View Androgel Review and Androgel Label ), ZESTORETIC (1/2 Tablet, Daily) (View Zestoretic Review and Zestoretic Label ), XALATAN (1 Gtt, Each Eye, Qpm) (View Xalatan Review and Xalatan Label ), VYTORIN (20 Mg, Daily) (View Vytorin Review and Vytorin Label ), MULTIVITAMIN /00831701/ (1 Tablet, Daily) (View Multivitamin /00831701/ Review and Multivitamin /00831701/ Label ), GLUCOSAMINE /CHOND/MSM /03040701/ (2 Tablet, Daily) (View Glucosamine /chond/msm /03040701/ Review and Glucosamine /chond/msm /03040701/ Label ), NEXIUM (40 Mg, Daily) (View Nexium Review and Nexium Label ).

5873687-4 | Abnormal Behaviour, Hallucination
Adverse event was reported on Sep 01, 2008 by a Male patient taking Androderm (View Usage) (Dosage: 2.5mg Per Day) . Location: UNITED KINGDOM , 52 years of age, weighting 229.3 lb, After Androderm was administered, patient had the following side effects: abnormal behaviour, hallucination. During the same period patient was treated with SERETIDE (2puff Twice Per Day) (View Seretide Review and Seretide Label ), SALAMOL (View Salamol Review and Salamol Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

5852643-6 | Abnormal Behaviour, Hallucination
on Aug 12, 2008 Male patient from UNITED KINGDOM , 52 years of age, was treated with Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: abnormal behaviour, hallucination. Androderm dosage: 2.5mg Per Day. During the same period patient was treated with SERETIDE (2puff Twice Per Day) (View Seretide Review and Seretide Label ), SALAMOL (View Salamol Review and Salamol Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ).

5845141-7 | Application Site Burn, Application Site Rash
on Aug 13, 2008 Male patient from UNITED STATES , 67 years of age, weighting 215.0 lb, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). Patient had the following side effects: application site burn, application site rash. Androderm dosage: One 1 Per Day Transdermal.

5838037-8 | Anger, Asthenia, Loss Of Libido
Patient was taking Androderm (View Usage). After Androderm was administered, patient had the following side effects: anger, asthenia, loss of libido on Mar 14, 2008 from UNITED STATES Additional patient health information: Male patient , 58 years of age, weighting 160.3 lb, was diagnosed with depression (What is depression?) and. Androderm dosage: 5mg Per Day. During the same period patient was treated with PAXIL (30mg Per Day) (View Paxil Review and Paxil Label ).

5837985-2 | Fatigue
Adverse event was reported on Jan 15, 2008 by a Male patient taking Androderm (View Usage) (Dosage: 5mg Per Day) was diagnosed with stress (What is stress?) and. Location: UNITED STATES , 59 years of age, Patient experienced the following unwanted or unexpected effects: fatigue. During the same period patient was treated with PAROXETINE HCL (10mg Per Day) (View Paroxetine Hcl Review and Paroxetine Hcl Label ).

5835565-6 | Abnormal Behaviour, Hallucination
on Jul 31, 2008 Male patient from UNITED KINGDOM , 52 years of age, was treated with Androderm (View Usage). Patient had the following side effects: abnormal behaviour, hallucination. Androderm dosage: 2.5mg Per Day. During the same period patient was treated with SERETIDE (2puff Twice Per Day) (View Seretide Review and Seretide Label ), SALAMOL (View Salamol Review and Salamol Label ), SPIRIVA (View Spiriva Review and Spiriva Label ).

5787221-0 | Application Site Reaction, Rash Erythematous
on Jun 23, 2008 Male patient from UNITED STATES , weighting 304.0 lb, was diagnosed with hypogonadism and was treated with Androderm (View Usage). After Androderm was administered, patient had the following side effects: application site reaction, rash erythematous. Androderm dosage: 5 Mg Q Am Transdermal. During the same period patient was treated with PROSCAR (View Proscar Review and Proscar Label ), BENICAR (View Benicar Review and Benicar Label ), DOXAZOSIN MESYLATE (View Doxazosin Mesylate Review and Doxazosin Mesylate Label ), METOPROLOL SUCCINATE (View Metoprolol Succinate Review and Metoprolol Succinate Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LIPITOR (View Lipitor Review and Lipitor Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), DILTIAZEM CD (View Diltiazem Cd Review and Diltiazem Cd Label ).

5735463-2 | Acromegaly, Erectile Dysfunction, Neoplasm Recurrence, Pituitary Tumour Benign
Patient was taking Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: acromegaly, erectile dysfunction (What is erectile dysfunction?), neoplasm recurrence, pituitary tumour benign on Apr 28, 2008 from UNITED STATES Additional patient health information: Male patient , 54 years of age, weighting 299.8 lb, was diagnosed with blood testosterone decreased and. Androderm dosage: Daily, Transdermal. During the same period patient was treated with ANDROGEL (7.5 G, Daily Via Pump, Topical; 5 G, Daily Via Pump, Topical) (View Androgel Review and Androgel Label ), OLMESARTAN (OLMESARTAN) (View Olmesartan (olmesartan) Review and Olmesartan (olmesartan) Label ), VARDENAFIL (VARDENAFIL) (View Vardenafil (vardenafil) Review and Vardenafil (vardenafil) Label ).

5580998-9 | Hepatic Adenoma, Hepatic Haemorrhage
Adverse event was reported on Dec 19, 2007 by a Male patient taking Androderm (View Usage) (Dosage: ) . Location: AUSTRALIA , 31 years of age, Patient had the following side effects: hepatic adenoma, hepatic haemorrhage. Patient was hospitalized.

5578870-3 | Nephroblastoma
on Dec 19, 2007 Male patient from UNITED STATES , 38 years of age, was treated with Androderm (View Usage). After Androderm was administered, patient had the following side effects: nephroblastoma. Androderm dosage: Oral. During the same period patient was treated with METHANDROSTENOLONE (Intramuscular) (View Methandrostenolone Review and Methandrostenolone Label ). Patient was hospitalized.

5541905-8 | Abdominal Pain Upper, Circulatory Collapse, Haemorrhage, Hepatic Adenoma, Hepatic Rupture, Renal Failure Acute, Sepsis
on Nov 21, 2007 Male patient from UNITED KINGDOM , 43 years of age, was treated with Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, circulatory collapse, haemorrhage, hepatic adenoma, hepatic rupture, renal failure acute, sepsis (What is sepsis?). Androderm dosage: . During the same period patient was treated with NANDROLONE DECANOATE (View Nandrolone Decanoate Review and Nandrolone Decanoate Label ), STANOZOLOL (View Stanozolol Review and Stanozolol Label ), PRIMABOLIN() (View Primabolin() Review and Primabolin() Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ). Patient was hospitalized.

5533884-4 | Connective Tissue Disorder, Peripheral Coldness, Skin Discolouration, Vasculitis
Patient was taking Androderm (View Usage). Patient had the following side effects: connective tissue disorder (What is connective tissue disorder?), peripheral coldness, skin discolouration, vasculitis (What is vasculitis?) on Nov 20, 2007 from UNITED KINGDOM Additional patient health information: Female patient , 43 years of age, was diagnosed with loss of libido and. Androderm dosage: 300 Mcg, Q24h, Transdermal. During the same period patient was treated with BECLOMETHASONE DIPROPIONATE (View Beclomethasone Dipropionate Review and Beclomethasone Dipropionate Label ), SALBUTAMOL SULFATE (SALBUTAMOL SULFATE) (View Salbutamol Sulfate (salbutamol Sulfate) Review and Salbutamol Sulfate (salbutamol Sulfate) Label ), OESTRADIOL (View Oestradiol Review and Oestradiol Label ).

5513639-7 | Endometrial Cancer Stage I
Adverse event was reported on Oct 31, 2007 by a Female patient taking Androderm (View Usage) (Dosage: Troche) was diagnosed with hypogonadism male and. Location: AUSTRALIA , 59 years of age, After Androderm was administered, patient had the following side effects: endometrial cancer stage i. During the same period patient was treated with PROGESTERONE IN OIL INJ (Troche) (View Progesterone In Oil Inj Review and Progesterone In Oil Inj Label ), ESTRADIOL (Troche) (View Estradiol Review and Estradiol Label ), DHEA(PRASTERONE) (Troche) (View Dhea(prasterone) Review and Dhea(prasterone) Label ).

5513589-6 | Endometrial Cancer Stage I
on Oct 31, 2007 Female patient from AUSTRALIA , 71 years of age, was treated with Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: endometrial cancer stage i. Androderm dosage: 0.188 Mg, Qam, + 0.375mg Qpm, 2.25 Mg Daily. During the same period patient was treated with PROGESTERONE IN OIL INJ (37.5 Mg Qam + 75mg Qpm Troche) (View Progesterone In Oil Inj Review and Progesterone In Oil Inj Label ), ESTRADIOL (0.875 Mg, Daily, 0.375 Mg, Qam + 0.75 Mg Qpm) (View Estradiol Review and Estradiol Label ), DHEA(PRASTERONE) 5MG (0.625 Mg, Qam + 1.25mg Qpm, 2.5 Mg, Daily) (View Dhea(prasterone) 5mg Review and Dhea(prasterone) 5mg Label ), ESTRONE (0.375 Mg, Qam + 0.75mg Qpm) (View Estrone Review and Estrone Label ).

5513538-0 | Endometrial Cancer Stage I
on Oct 31, 2007 Female patient from AUSTRALIA , 54 years of age, was treated with Androderm (View Usage). Patient had the following side effects: endometrial cancer stage i. Androderm dosage: Troche. During the same period patient was treated with PROGESTERONE IN OIL INJ (Troche) (View Progesterone In Oil Inj Review and Progesterone In Oil Inj Label ), ESTRADIOL (Troche) (View Estradiol Review and Estradiol Label ), ESTRONE (Troche) (View Estrone Review and Estrone Label ), ESTRIOL (ESTRIOL) (Troche) (View Estriol (estriol) Review and Estriol (estriol) Label ), DHEA(PRASTERONE) (Troche) (View Dhea(prasterone) Review and Dhea(prasterone) Label ).

5246418-9 | Application Site Excoriation, Application Site Exfoliation
Patient was taking Androderm (View Usage). After Androderm was administered, patient had the following side effects: application site excoriation, application site exfoliation on Feb 22, 2007 from UNITED STATES Additional patient health information: Male patient , 63 years of age, weighting 145.0 lb, was diagnosed with blood testosterone decreased and. Androderm dosage: 1 Patch Daily.

5164906-0 | Lymphangitis
Adverse event was reported on Nov 16, 2006 by a Female patient taking Androderm (View Usage) (Dosage: 10 Mg, X 1 Day, Transdermal) was diagnosed with organic erectile dysfunction and. Location: SPAIN , 58 years of age, Patient experienced the following unwanted or unexpected effects: lymphangitis. During the same period patient was treated with LEVITRA (10 Mg, X 1 Day, Oral) (View Levitra Review and Levitra Label ), NITROGLYCERIN SLOVAKOFARMA (GLYCERYL TRINITRATE) (View Nitroglycerin Slovakofarma (glyceryl Trinitrate) Review and Nitroglycerin Slovakofarma (glyceryl Trinitrate) Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

5152092-2 | Asthenia, Blood Testosterone Decreased, Libido Decreased
on Nov 13, 2006 Male patient from UNITED STATES , 58 years of age, was diagnosed with blood testosterone and was treated with Androderm (View Usage). Patient had the following side effects: asthenia, blood testosterone decreased, libido decreased. Androderm dosage: Apply One Patch Daily.

5129528-6 | Malignant Melanoma
on Oct 02, 2006 Male patient from UNITED STATES , 57 years of age, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). After Androderm was administered, patient had the following side effects: malignant melanoma. Androderm dosage: 1 Patch, Daily, Transdermal.

5108917-X | Burns Third Degree, Caustic Injury
Patient was taking Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: burns third degree, caustic injury on Sep 15, 2006 from UNITED STATES Additional patient health information: Male patient , weighting 145.0 lb, . Androderm dosage: 5 Mg Q Am Transdermal. During the same period patient was treated with LEVOXYL (View Levoxyl Review and Levoxyl Label ), NORVASC (View Norvasc Review and Norvasc Label ), NORPACE (View Norpace Review and Norpace Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LIPITOR (View Lipitor Review and Lipitor Label ), SINGULAIR (View Singulair Review and Singulair Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

5055873-9 | Skin Reaction
Adverse event was reported on Jul 17, 2006 by a Male patient taking Androderm (View Usage) (Dosage: One Daily Top) . Location: UNITED STATES , weighting 150.0 lb, Patient had the following side effects: skin reaction.

5007484-9 | Aggression, Antisocial Behaviour, Confusional State, Depression Suicidal, Fear, Incorrect Dose Administered, Thinking Abnormal
on May 05, 2006 Male patient from UNITED STATES , 54 years of age, was diagnosed with blood testosterone decreased and was treated with Androderm (View Usage). After Androderm was administered, patient had the following side effects: aggression, antisocial behaviour, confusional state, depression suicidal, fear, incorrect dose administered, thinking abnormal. Androderm dosage: 2 Patch, Daily, Transdermal. During the same period patient was treated with VIAGRA (View Viagra Review and Viagra Label ), GLUCOVANCE (View Glucovance Review and Glucovance Label ), ACTOS (View Actos Review and Actos Label ).

4942603-1 | Aggression, Alcoholism, Anger, Bipolar I Disorder, Legal Problem, Physical Abuse, Thinking Abnormal
on Feb 28, 2006 Male patient from UNITED STATES , 41 years of age, was diagnosed with blood testosterone decreased, muscle mass and was treated with Androderm (View Usage). Patient experienced the following unwanted or unexpected effects: aggression, alcoholism (What is alcoholism?), anger, bipolar i disorder, legal problem, physical abuse, thinking abnormal. Androderm dosage: 1 Patch Q 24 Hrs Or Q 48 Hrs, Transdermal. Patient was hospitalized.

4866538-8 | Aggression, Antisocial Behaviour, Depression Suicidal, Fear, Incorrect Dose Administered
Patient was taking Androderm (View Usage). Patient had the following side effects: aggression, antisocial behaviour, depression suicidal, fear, incorrect dose administered on Dec 12, 2003 from UNITED STATES Additional patient health information: Male patient , 54 years of age, was diagnosed with blood testosterone decreased and. Androderm dosage: 2 Patch, Daily, Transdermal. During the same period patient was treated with VIAGRA (View Viagra Review and Viagra Label ), GLUCOVANCE (GLIBENCLAMIDE) (View Glucovance (glibenclamide) Review and Glucovance (glibenclamide) Label ), ACTOS/USA/ (PIOGLITAZONE HYDROCHLORIDE) (View Actos/usa/ (pioglitazone Hydrochloride) Review and Actos/usa/ (pioglitazone Hydrochloride) Label ).