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Fosamax Side Effects Report #5648917-4
Health Professional from UNITED STATES reported FOSAMAX problem on Feb 26, 2008. Female patient, 54 years of age, was diagnosed with osteoporosis, pain management and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, anxiety, back injury, depression, fungal infection, increased tendency to bruise, intervertebral disc disorder, intervertebral disc protrusion, malignant melanoma, . FOSAMAX dosage: unknown. During the same period patient was treated with HYDROCODONE BITARTRATE, AMOXICILLIN. Patient recovered.

Fosamax Side Effects Report #5662934-X
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Mar 03, 2008. Male patient, 70 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, adverse event, allergic granulomatous angiitis, allergy to vaccine, anaemia, bursitis, candidiasis, cataract nuclear, clostridium difficile colitis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5674759-X
Physician from UNITED STATES reported FOSAMAX problem on Mar 10, 2008. Female patient, 67 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, alcoholism, atelectasis, balance disorder, bone density decreased, bronchiectasis, bronchitis chronic, bursitis, cardiac flutter, . FOSAMAX dosage: unknown. During the same period patient was treated with ZOLOFT, LIPITOR, ZANTAC, CLARITIN, NASACORT, SYNTHROID, PREMARIN. Patient was hospitalized and became disabled. Patient recovered.

Avonex Side Effects Report #5683506-7
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 14, 2008. Female patient was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, basal cell carcinoma, . AVONEX dosage: unknown. Patient recovered.


Remicade Side Effects Report #5613654-9
Health Professional from CANADA reported REMICADE problem on Jan 29, 2008. Female patient, weighting 115.1 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, . REMICADE dosage: unknown. During the same period patient was treated with CELEBREX, ACTONEL, CALCIUM GLUCONATE, METHOTREXATE, FOLIC ACID, VITAMIN D. Patient recovered.

Sti Side Effects Report #5615937-5
STI problem was reported by a Physician from GERMANY on Feb 01, 2008. Male patient, 64 years of age, was diagnosed with chronic myeloid leukaemia and was treated with STI. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, basal cell carcinoma, malignant tumour excision, skin lesion, squamous cell carcinoma of skin, . STI dosage: 600 MG, QD. Patient recovered.

Fosamax Side Effects Report #5619188-X
Health Professional from UNITED STATES reported FOSAMAX problem on Jan 29, 2008. Male patient, 70 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, allergy to vaccine, bursitis, cataract nuclear, clostridium difficile colitis, cognitive disorder, cryptogenic organising pneumonia, dermatitis allergic, erectile dysfunction, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5629750-6
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Feb 06, 2008. Male patient, 70 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, allergy to vaccine, bursitis, cataract nuclear, clostridium difficile colitis, cognitive disorder, cryptogenic organising pneumonia, dermatitis allergic, erectile dysfunction, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5632137-3
Health Professional from UNITED STATES reported FOSAMAX problem on Feb 13, 2008. Female patient, 54 years of age, was diagnosed with osteoporosis, pain management and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, anxiety, back injury, depression, fungal infection, increased tendency to bruise, intervertebral disc disorder, intervertebral disc protrusion, malignant melanoma, . FOSAMAX dosage: unknown. During the same period patient was treated with HYDROCODONE BITARTRATE, AMOXICILLIN. Patient recovered.


Fosamax Side Effects Report #5645373-7
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Feb 19, 2008. Male patient, 70 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, adverse event, allergy to vaccine, bursitis, cataract nuclear, clostridium difficile colitis, cognitive disorder, cryptogenic organising pneumonia, dermatitis allergic, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5585623-9
Health Professional from UNITED STATES reported FOSAMAX problem on Jan 03, 2008. Male patient, 70 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, bursitis, cataract nuclear, clostridium difficile colitis, cognitive disorder, cryptogenic organising pneumonia, dermatitis allergic, erectile dysfunction, gastrooesophageal reflux disease, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5595289-X
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Jan 11, 2008. Female patient, 77 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, anxiety, aphthous stomatitis, bone disorder, bursa disorder, eye disorder, fear, oral disorder, osteonecrosis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5598526-0
Physician from NETHERLANDS reported REMICADE problem on Jan 15, 2008. Female patient was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, squamous cell carcinoma, . REMICADE dosage: unknown. During the same period patient was treated with PREDNISONE, IMURAN. Patient recovered.

Fosamax Side Effects Report #5604561-6
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Jan 18, 2008. Male patient, 70 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, bursitis, cataract nuclear, clostridium difficile colitis, cognitive disorder, cryptogenic organising pneumonia, dermatitis allergic, erectile dysfunction, gastrooesophageal reflux disease, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.


Fosamax Side Effects Report #5552371-0
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Dec 03, 2007. Male patient, 70 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, bursitis, cataract nuclear, clostridium difficile colitis, cognitive disorder, cryptogenic organising pneumonia, dermatitis allergic, erectile dysfunction, gastrooesophageal reflux disease, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Lescol Side Effects Report #5519143-4
LESCOL problem was reported by a Physician from FRANCE on Nov 08, 2007. Male patient, 78 years of age, was treated with LESCOL. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, anaemia, eczema, myelofibrosis, osteoarthritis, red blood cell morphology abnormal, toxic skin eruption, . LESCOL dosage: unknown. Patient recovered.

Lescol Side Effects Report #5519866-7
Physician from FRANCE reported LESCOL problem on Nov 08, 2007. Male patient, 78 years of age, was treated with LESCOL. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, anaemia, eczema, myelofibrosis, osteoarthritis, red blood cell morphology abnormal, toxic skin eruption, . LESCOL dosage: unknown. Patient recovered.

Lescol Side Effects Report #5520106-3
LESCOL problem was reported by a Physician from FRANCE on Nov 08, 2007. Male patient, 78 years of age, was treated with LESCOL. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, anaemia, eczema, myelofibrosis, osteoarthritis, red blood cell morphology abnormal, toxic skin eruption, . LESCOL dosage: unknown. Patient recovered.

Merrem Side Effects Report #5479343-9
Pharmacist from UNITED STATES reported MERREM problem on Oct 04, 2007. Male patient, 37 years of age, weighting 181.4 lb, was diagnosed with pneumonia and was treated with MERREM. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, . MERREM dosage: unknown. During the same period patient was treated with PROTONIX, COUMADIN, LASIX, ZONEGRAN, VALPROIC ACID, REGLAN, VANCOMYCIN. Patient was hospitalized. Patient recovered.


Prograf Side Effects Report #5501370-3
PROGRAF problem was reported by a Physician from FRANCE on Oct 10, 2007. Male patient, 69 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, basal cell carcinoma, liver disorder, neoplasm recurrence, neuroendocrine carcinoma of the skin, sepsis, skin graft, squamous cell carcinoma, . PROGRAF dosage: 0.5 MG, BID; 1 MG, UID/QD. During the same period patient was treated with PREDNISONE. Patient died on 09/01/2006.

Efudex Side Effects Report #5459394-0
Consumer or non-health professional from UNITED STATES reported EFUDEX problem on Sept 11, 2007. Female patient, 67 years of age, weighting 150.0 lb, was diagnosed with osteoporosis and was treated with EFUDEX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, dermatitis contact, ephelides, rash papular, squamous cell carcinoma of skin, . EFUDEX dosage: unknown. During the same period patient was treated with RETIN, FORTEO. Patient recovered.

Donepezil Side Effects Report #5463599-2
DONEPEZIL problem was reported by a Physician from UNITED STATES on Sept 12, 2007. Male patient, 73 years of age, weighting 185.4 lb, was diagnosed with dementia alzheimer's type and was treated with DONEPEZIL. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, basal cell carcinoma, seborrhoeic keratosis, . DONEPEZIL dosage: 10 MG, 1IN 1 D, PER ORAL. During the same period patient was treated with CENTRUM SILVER, VITAMIN C, VITAMIN E. Patient recovered.

Fosamax Side Effects Report #5755584-8
Physician from UNITED STATES reported FOSAMAX problem on May 21, 2008. Female patient, 67 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, alcoholism, atelectasis, balance disorder, bone density decreased, bronchiectasis, bronchitis chronic, bursitis, cardiac flutter, . FOSAMAX dosage: unknown. During the same period patient was treated with ZOLOFT, LIPITOR, ZANTAC, CLARITIN, NASACORT, SYNTHROID, PREMARIN. Patient was hospitalized and became disabled. Patient recovered.

Humira Side Effects Report #5771116-2
HUMIRA problem was reported by a Physician from UNITED STATES on May 21, 2008. Male patient, weighting 165.1 lb, was diagnosed with psoriasis, arthritis, asthma and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, psoriasis, . HUMIRA dosage: unknown. During the same period patient was treated with ULOBETASOL PROPIONATE, CALCIPOTRIENE, TACLONEX, NEBUTONE. Patient recovered.

Lamictal Side Effects Report #5776883-X
Consumer or non-health professional from UNITED STATES reported LAMICTAL problem on June 11, 2008. Female patient, 63 years of age, was diagnosed with depression and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, collagen-vascular disease, dry eye, dyshidrosis, erythema, erythema multiforme, leukocytoclastic vasculitis, . LAMICTAL dosage: unknown. During the same period patient was treated with PREVACID, VIVELLE, ADVAIR DISKUS, BENICAR, ZANTAC, LORAZEPAM, MAGIC MOUTHWASH, WELLBUTRIN. Patient was hospitalized. Patient recovered.

Mabthera Side Effects Report #5777873-3
MABTHERA problem was reported by a Physician from UNITED KINGDOM on June 05, 2008. Female patient was diagnosed with rheumatoid arthritis and was treated with MABTHERA. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, neoplasm, . MABTHERA dosage: unknown. During the same period patient was treated with PREDNISONE, METHOTREXATE, LEVOTHYROXINE, FOLIC ACID, ESOMEPRAZOLE MAGNESIUM, CALCIUM CARBONATE. Patient recovered.

Fosamax Side Effects Report #5792510-X
Health Professional from UNITED STATES reported FOSAMAX problem on June 18, 2008. Female patient, 86 years of age, was diagnosed with osteoporosis, scoliosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, carotid artery disease, fatigue, headache, hypothyroidism, infection, malaise, osteomyelitis, osteonecrosis, . FOSAMAX dosage: unknown. During the same period patient was treated with AMITRIPTYLINE, FOSAMAX PLUS D, SYNTHROID, CARISOPRODOL. Patient was hospitalized. Patient recovered.

Tysabri Side Effects Report #5792769-9
TYSABRI problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2008. Female patient, 47 years of age, weighting 180.0 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, amenorrhoea, skin lesion, squamous cell carcinoma, . TYSABRI dosage: 300 MG; QM; IV. Patient recovered.

Humira Side Effects Report #5793033-4
Health Professional from SWEDEN reported HUMIRA problem on June 19, 2008. Female patient, 63 years of age, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, basal cell carcinoma, skin cancer, . HUMIRA dosage: unknown. Patient was hospitalized. Patient recovered.

Clonidine Side Effects Report #5734185-1
CLONIDINE problem was reported by a Physician from UNITED STATES on May 01, 2008. Female patient, 63 years of age, weighting 172.0 lb, was diagnosed with hypertension and was treated with CLONIDINE. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, atrial fibrillation, blood pressure increased, bronchitis, cardiac pacemaker insertion, chronic obstructive pulmonary disease, coagulopathy, constipation, cough, . CLONIDINE dosage: 0.1 MG, BID. During the same period patient was treated with VERELAN, COUMADIN, MICARDIS, DARVON, ASPIRIN. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5745337-9
Physician from UNITED STATES reported FOSAMAX problem on May 12, 2008. Female patient, 83 years of age, was diagnosed with osteopenia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, carotid bruit, diarrhoea, fall, glucose tolerance impaired, infection, nausea, nerve injury, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5745342-2
FOSAMAX problem was reported by a Health Professional from UNITED STATES on May 14, 2008. Male patient, 70 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, adverse event, allergic granulomatous angiitis, allergy to vaccine, anaemia, bursitis, candidiasis, cataract nuclear, clostridium difficile colitis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Femara Side Effects Report #5750110-1
Consumer or non-health professional from UNITED STATES reported FEMARA problem on May 22, 2008. Female patient, weighting 282.6 lb, was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, condition aggravated, psoriasis, . FEMARA dosage: 2.5 MG. During the same period patient was treated with ACTOS, ASACOL, BENICAR, CALCIUM, CARDIZEM, CENTRUM SILVER, FISH OIL CAPSULES, HYDROCHLOROTHIAZIDE. Patient recovered.

Omalizumab Side Effects Report #5691127-5
OMALIZUMAB problem was reported by a Consumer or non-health professional from SWITZERLAND on Mar 17, 2008. Male patient, weighting 174.2 lb, was diagnosed with asthma and was treated with OMALIZUMAB. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, . OMALIZUMAB dosage: 150 MG, Q4W. Patient recovered.

Fosamax Side Effects Report #5699949-1
Health Professional from UNITED STATES reported FOSAMAX problem on Apr 03, 2008. Female patient, 54 years of age, was diagnosed with osteoporosis, pain management and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, anxiety, back injury, depression, fungal infection, increased tendency to bruise, intervertebral disc disorder, intervertebral disc protrusion, malignant melanoma, . FOSAMAX dosage: unknown. During the same period patient was treated with HYDROCODONE BITARTRATE, AMOXICILLIN, MAXZIDE, VICODIN. Patient recovered.

Sorafenib Side Effects Report #5709392-4
SORAFENIB problem was reported by a Health Professional from UNITED STATES on Apr 14, 2008. Female patient was treated with SORAFENIB. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, rash, squamous cell carcinoma, . SORAFENIB dosage: TOTAL DAILY DOSE: 800 MG UNIT DOSE: 200 MG. Patient recovered.

Nutropin Side Effects Report #5710479-0
Consumer or non-health professional from UNITED STATES reported NUTROPIN AQ problem on Apr 09, 2008. Female patient was diagnosed with growth hormone deficiency and was treated with NUTROPIN AQ. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, . NUTROPIN AQ dosage: 0.2 ML, QD. During the same period patient was treated with ESTRADIOL, PROGESTERONE, THYROID. Patient recovered.

Cyclosporine Side Effects Report #5711698-X
CYCLOSPORINE problem was reported by a Health Professional from DENMARK on Apr 14, 2008. Male patient, 46 years of age, was diagnosed with renal transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, basal cell carcinoma, bowen's disease, chronic allograft nephropathy, complications of transplanted kidney, erysipelas, impaired healing, lymphangiosis carcinomatosa, . CYCLOSPORINE dosage: 5 MG/KG/D. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISOLONE, SIROLIMUS. Patient died on 12/01/2006.

Fosamax Side Effects Report #5712923-1
Physician from UNITED STATES reported FOSAMAX problem on Apr 14, 2008. Female patient, 67 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, alcoholism, atelectasis, balance disorder, bone density decreased, bronchiectasis, bronchitis chronic, bursitis, cardiac flutter, . FOSAMAX dosage: unknown. During the same period patient was treated with ZOLOFT, LIPITOR, ZANTAC, CLARITIN, NASACORT, SYNTHROID, PREMARIN. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5719838-3
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Apr 15, 2008. Male patient, 70 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, adverse event, allergic granulomatous angiitis, allergy to vaccine, anaemia, bursitis, candidiasis, cataract nuclear, clostridium difficile colitis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5721322-8
Physician from DENMARK reported CYCLOSPORINE problem on Apr 16, 2008. Male patient, 46 years of age, was diagnosed with immunosuppression and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, basal cell carcinoma, bowen's disease, chronic allograft nephropathy, complications of transplanted kidney, erysipelas, impaired healing, lymphangiosis carcinomatosa, lymphangitis, . CYCLOSPORINE dosage: 5 MG/KG. During the same period patient was treated with SIROLIMUS. Patient died on 12/01/2006.

Humira Side Effects Report #5354697-2
HUMIRA problem was reported by a Health Professional from UNITED KINGDOM on June 06, 2007. Female patient, 60 years of age, weighting 198.4 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, basal cell carcinoma, . HUMIRA dosage: unknown. Patient recovered.

Sti Side Effects Report #5360622-0
Physician from GERMANY reported STI problem on June 07, 2007. Male patient, 64 years of age, was diagnosed with chronic myeloid leukaemia and was treated with STI. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, malignant tumour excision, squamous cell carcinoma of skin, . STI dosage: 600 MG, QD. Patient recovered.

Sti Side Effects Report #5360624-4
STI problem was reported by a Physician from GERMANY on June 07, 2007. Male patient, 64 years of age, was diagnosed with chronic myeloid leukaemia and was treated with STI. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, malignant tumour excision, squamous cell carcinoma of skin, . STI dosage: 600 MG, QD. Patient recovered.

Diclofenac Side Effects Report #5364686-X
Health Professional from GERMANY reported DICLOFENAC problem on June 18, 2007. Male patient, 69 years of age, was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, erythema, inflammation, oedema, secretion discharge, skin exfoliation, . DICLOFENAC dosage: unknown. Patient recovered.

Diclofenac Side Effects Report #5364795-5
DICLOFENAC problem was reported by a Health Professional from GERMANY on June 18, 2007. Male patient, 69 years of age, was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, erythema, inflammation, oedema, secretion discharge, skin exfoliation, . DICLOFENAC dosage: unknown. Patient recovered.

Diclofenac Side Effects Report #5364801-8
Health Professional from GERMANY reported DICLOFENAC problem on June 18, 2007. Male patient, 72 years of age, was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, erythema, inflammation, oedema, secretion discharge, skin exfoliation, . DICLOFENAC dosage: unknown. Patient recovered.

Diclofenac Side Effects Report #5364821-3
DICLOFENAC problem was reported by a Health Professional from GERMANY on June 18, 2007. Male patient, 70 years of age, was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, erythema, inflammation, oedema, secretion discharge, skin exfoliation, . DICLOFENAC dosage: unknown. Patient recovered.

Diclofenac Side Effects Report #5364829-8
Health Professional from GERMANY reported DICLOFENAC problem on June 18, 2007. Male patient, 72 years of age, was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, erythema, inflammation, oedema, secretion discharge, skin exfoliation, . DICLOFENAC dosage: unknown. Patient recovered.

Fluoxetine Side Effects Report #5337055-6
FLUOXETINE problem was reported by a Physician from GERMANY on May 16, 2007. Female patient, 55 years of age, was diagnosed with depression and was treated with FLUOXETINE. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, blood immunoglobulin a decreased, blood immunoglobulin g decreased, blood immunoglobulin m decreased, squamous cell carcinoma, . FLUOXETINE dosage: 20 MG, DAILY (1/D). During the same period patient was treated with CORTICOSTEROID NOS, TAVOR. Patient recovered.

Rogaine Side Effects Report #5339574-5
Consumer or non-health professional from UNITED STATES reported ROGAINE problem on May 07, 2007. Male patient, 80 years of age, weighting 192.0 lb, was diagnosed with alopecia and was treated with ROGAINE. After drug was administered, patient experienced the following problems/side effects: actinic keratosis, erythema, hypoaesthesia, hypoaesthesia facial, insomnia, multiple lentigines syndrome, pain of skin, pigmentation disorder, pruritus, . ROGAINE dosage: ONE ML TWICE DAILY (2 IN 1 D), TOPICAL. During the same period patient was treated with LEVOTHYROXINE, ASPIRIN, FELODIPINE, ATORVASTATIN CALCIUM, VITAMIN E, FOLIC ACID, INSULIN. Patient recovered.