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BLOOD IRON DECREASED side effect

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Advair Side Effects Report #5663109-0
Consumer or non-health professional from UNITED STATES reported ADVAIR DISKUS problem on Mar 05, 2008. Female patient, 82 years of age, was diagnosed with asthma and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, blood potassium decreased, bronchospasm, dyspnoea, vertigo, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with XOPENEX, SYMBICORT, OXYGEN, DIOVAN, SYNTHROID, PREDNISONE. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5665139-1
FOSAMAX problem was reported by a Physician from UNITED KINGDOM on Mar 07, 2008. Female patient, 70 years of age, was diagnosed with osteoporosis, blood cholesterol increased, hypothyroidism and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, blood thyroid stimulating hormone decreased, bruxism, edentulous, jaw disorder, melanocytic naevus, mitral valve prolapse, osteonecrosis, road traffic accident, . FOSAMAX dosage: unknown. During the same period patient was treated with RISEDRONATE, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5611644-3
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on Jan 22, 2008. Male patient, weighting 170.4 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, hypersensitivity, self injurious behaviour, suicide attempt, . CHANTIX dosage: unknown. During the same period patient was treated with KLONOPIN, CYMBALTA. Patient was hospitalized. Patient recovered.

Xopenex Side Effects Report #5632531-0
XOPENEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 04, 2008. Female patient, 82 years of age, was diagnosed with asthma, chronic obstructive pulmonary disease and was treated with XOPENEX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, blood potassium decreased, dyspnoea, vertigo, . XOPENEX dosage: 1.25 MG/3ML; BID; INHALATION; 1.25 MG/3ML; BID; INHALATION. During the same period patient was treated with ADVAIR DISKUS, SYMBICORT, OXYGEN, DIOVAN. Patient was hospitalized. Patient recovered.


Duragesic Side Effects Report #5636099-4
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Feb 14, 2008. Male patient, weighting 140.0 lb, was diagnosed with pain, hypertension, depression, blood cholesterol increased, blood pressure, gastrooesophageal reflux disease and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, decreased appetite, dementia, insomnia, muscle spasms, . DURAGESIC dosage: unknown. During the same period patient was treated with LISINOPRIL, LEXAPRO, LYRICA, ASPIRIN, SIMVASTATIN, AMLODIPINE, NEXIUM, VITAMIN CAP. Patient recovered.

Plavix Side Effects Report #5622439-9
PLAVIX problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 01, 2007. Female patient, 78 years of age, was diagnosed with stent placement and was treated with PLAVIX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, gastric ulcer haemorrhage, myocardial infarction, . PLAVIX dosage: 75 MG QD - ORAL. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, LEVOTHYROXINE, OLMESARTAN MEDOXOMIL, FUROSEMIDE, PIOGLITAZONE, ENALAPRIL MALEATE, METOPROLOL SUCCINATE, PREGABALIN. Patient recovered.

Revlimid Side Effects Report #5632526-7
Pharmacist from UNITED STATES reported REVLIMID problem on Oct 09, 2007. Female patient, 63 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, blood magnesium decreased, . REVLIMID dosage: 10 MG, 1 IN 1 D, ORAL. Patient recovered.

Byetta Side Effects Report #5651796-2
BYETTA problem was reported by a Health Professional from UNITED STATES on Oct 24, 2007. Female patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemoglobin decreased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE. Patient recovered.

Avonex Side Effects Report #5526049-3
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Nov 13, 2007. Female patient, 42 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, injection site infection, pyrexia, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.


Duragesic Side Effects Report #5528702-4
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 19, 2007. Female patient, weighting 135.0 lb, was diagnosed with pain, hypothyroidism, sleep disorder and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, blood potassium decreased, eating disorder, hypothyroidism, oral intake reduced, unevaluable event, . DURAGESIC dosage: unknown. During the same period patient was treated with SYNTHROID, XANAX, RESTORIL, VOLTAREN. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5475669-3
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Sept 21, 2007. Female patient, 42 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, injection site infection, pyrexia, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Zocor Side Effects Report #5484443-3
ZOCOR problem was reported by a Physician from UNITED KINGDOM on Oct 03, 2007. Male patient, 63 years of age, was diagnosed with prophylaxis, hypertension and was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemoglobin decreased, hepatic function abnormal, hypertension, . ZOCOR dosage: unknown. During the same period patient was treated with RAMIPRIL, AMLODIPINE BESYLATE. Patient recovered.

Humira Side Effects Report #5499884-8
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Oct 16, 2007. Female patient, weighting 185.2 lb, was diagnosed with crohn's disease, pregnancy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemorrhage, labour complication, nasopharyngitis, pyrexia, streptococcal identification test positive, urinary tract infection, vulvovaginal mycotic infection, . HUMIRA dosage: unknown. During the same period patient was treated with PRENATAL VITAMINS, PRENATAL VITAMINS, REMICADE, PREDNISONE. Patient recovered.

Cytotec Side Effects Report #5475594-8
CYTOTEC problem was reported by a Physician from UNITED STATES on Mar 05, 2007. Female patient, 19 years of age, was diagnosed with abortion induced and was treated with CYTOTEC. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, dizziness, haemoglobin decreased, metrorrhagia, vaginal discharge, vaginal haemorrhage, . CYTOTEC dosage: unknown. Patient recovered.


Namenda Side Effects Report #5419211-1
Consumer or non-health professional from UNITED STATES reported NAMENDA problem on Aug 06, 2007. Female patient, 80 years of age, was diagnosed with dementia alzheimer's type, osteoporosis and was treated with NAMENDA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, joint swelling, oedema peripheral, renal impairment, . NAMENDA dosage: 5 MG BID PO. During the same period patient was treated with BONIVA, MUCINEX, LOTREL, POTASSIUM CHLORIDE, PAXIL. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5423078-5
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 13, 2007. Female patient, 40 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haematocrit decreased, menorrhagia, . REBIF dosage: unknown. During the same period patient was treated with SEDAPAP, LORCET, GABAPENTIN, EFFEXOR, KLONOPIN, TRAZODONE, ORAL CONTRACEPTIVE. Patient was hospitalized. Patient recovered.

Lithobid Side Effects Report #5380263-9
Consumer or non-health professional from TURKEY reported LITHOBID problem on June 19, 2007. Female patient, 54 years of age, was diagnosed with mania and was treated with LITHOBID. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, deep vein thrombosis, disorientation, extrapyramidal disorder, fibrin d dimer increased, fibrin degradation products increased, haemoglobin decreased, hypernatraemia, hyperthyroidism, . LITHOBID dosage: 1500; 1200 MG, QD. During the same period patient was treated with RISPERIDONE, BIPERIDEN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5383212-2
LYRICA problem was reported by a Consumer or non-health professional from UNITED STATES on June 28, 2007. Female patient, weighting 150.3 lb, was diagnosed with pain, anxiety and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, blood potassium decreased, bone pain, muscle spasms, myalgia, restless legs syndrome, . LYRICA dosage: unknown. During the same period patient was treated with VITAMIN, MORPHINE, CLONAZEPAM. Patient recovered.

Namenda Side Effects Report #5387181-0
Consumer or non-health professional from UNITED STATES reported NAMENDA problem on July 03, 2007. Female patient, 80 years of age, was diagnosed with dementia alzheimer's type, osteoporosis and was treated with NAMENDA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, joint swelling, oedema peripheral, renal impairment, . NAMENDA dosage: 5 MG BID PO. During the same period patient was treated with BONIVA, MUCINEX, LOTREL, POTASSIUM CHLORIDE, PAXIL. Patient was hospitalized. Patient recovered.


Lithium Side Effects Report #5391734-3
LITHIUM CARBONATE problem was reported by a Consumer or non-health professional from TURKEY on July 06, 2007. Female patient, 54 years of age, was diagnosed with mania and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, deep vein thrombosis, disorientation, extrapyramidal disorder, fibrin d dimer increased, fibrin degradation products increased, haemoglobin decreased, hypernatraemia, hyperthyroidism, . LITHIUM CARBONATE dosage: unknown. During the same period patient was treated with RISPERIDONE, BIPERIDEN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5399360-7
Consumer or non-health professional from UNITED STATES reported BONIVA problem on July 17, 2007. Female patient, 80 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, oedema peripheral, renal impairment, . BONIVA dosage: unknown. During the same period patient was treated with NAMENDA, MUCINEX, LOTREL, POTASSIUM CHLORIDE, PAXIL. Patient was hospitalized. Patient recovered.

Lithobid Side Effects Report #5380263-9
LITHOBID problem was reported by a Consumer or non-health professional from TURKEY on June 19, 2007. Female patient, 54 years of age, was diagnosed with mania and was treated with LITHOBID. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, deep vein thrombosis, disorientation, extrapyramidal disorder, fibrin d dimer increased, fibrin degradation products increased, haemoglobin decreased, hypernatraemia, hyperthyroidism, . LITHOBID dosage: 1500; 1200 MG, QD. During the same period patient was treated with RISPERIDONE, BIPERIDEN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5383212-2
Consumer or non-health professional from UNITED STATES reported LYRICA problem on June 28, 2007. Female patient, weighting 150.3 lb, was diagnosed with pain, anxiety and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, blood potassium decreased, bone pain, muscle spasms, myalgia, restless legs syndrome, . LYRICA dosage: unknown. During the same period patient was treated with VITAMIN, MORPHINE, CLONAZEPAM. Patient recovered.

Namenda Side Effects Report #5387181-0
NAMENDA problem was reported by a Consumer or non-health professional from UNITED STATES on July 03, 2007. Female patient, 80 years of age, was diagnosed with dementia alzheimer's type, osteoporosis and was treated with NAMENDA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, joint swelling, oedema peripheral, renal impairment, . NAMENDA dosage: 5 MG BID PO. During the same period patient was treated with BONIVA, MUCINEX, LOTREL, POTASSIUM CHLORIDE, PAXIL. Patient was hospitalized. Patient recovered.

Lithium Side Effects Report #5391734-3
Consumer or non-health professional from TURKEY reported LITHIUM CARBONATE problem on July 06, 2007. Female patient, 54 years of age, was diagnosed with mania and was treated with LITHIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, deep vein thrombosis, disorientation, extrapyramidal disorder, fibrin d dimer increased, fibrin degradation products increased, haemoglobin decreased, hypernatraemia, hyperthyroidism, . LITHIUM CARBONATE dosage: unknown. During the same period patient was treated with RISPERIDONE, BIPERIDEN HYDROCHLORIDE. Patient was hospitalized. Patient recovered.

Boniva Side Effects Report #5399360-7
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on July 17, 2007. Female patient, 80 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, oedema peripheral, renal impairment, . BONIVA dosage: unknown. During the same period patient was treated with NAMENDA, MUCINEX, LOTREL, POTASSIUM CHLORIDE, PAXIL. Patient was hospitalized. Patient recovered.

Lexapro Side Effects Report #5763211-9
Consumer or non-health professional from UNITED STATES reported LEXAPRO problem on May 29, 2008. Male patient, 44 years of age, was diagnosed with anxiety and was treated with LEXAPRO. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemoglobin decreased, miosis, pallor, . LEXAPRO dosage: 5 MG QD PO. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5772897-4
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2008. Female patient, 42 years of age, weighting 265.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, injection site infection, oedema peripheral, pyrexia, vaginal haemorrhage, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5774570-5
Consumer or non-health professional from UNITED STATES reported AVONEX problem on June 02, 2008. Female patient, 64 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemoglobin decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Zocor Side Effects Report #5786707-2
ZOCOR problem was reported by a Physician from UNITED KINGDOM on June 18, 2008. Male patient, 63 years of age, was diagnosed with prophylaxis, hypertension, cardiovascular event prophylaxis and was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemoglobin decreased, hepatic function abnormal, . ZOCOR dosage: unknown. During the same period patient was treated with RAMIPRIL, AMLODIPINE BESYLATE, ASPIRIN. Patient recovered.

Zocor Side Effects Report #5792514-7
Physician from UNITED KINGDOM reported ZOCOR problem on June 18, 2008. Male patient, 63 years of age, was diagnosed with prophylaxis, hypertension, cardiovascular event prophylaxis and was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemoglobin decreased, hepatic function abnormal, . ZOCOR dosage: unknown. During the same period patient was treated with RAMIPRIL, AMLODIPINE BESYLATE, ASPIRIN. Patient recovered.

Simvastatin Side Effects Report #5794427-3
SIMVASTATIN problem was reported by a Health Professional from UNITED KINGDOM on June 24, 2008. Female patient was diagnosed with prophylaxis, hypertension, cardiovascular event prophylaxis and was treated with SIMVASTATIN. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemoglobin decreased, hepatic function abnormal, . SIMVASTATIN dosage: 20 MG, QD. During the same period patient was treated with AMLODIPINE BESYLATE, ASPIRIN, RAMIPRIL, ATENOLOL. Patient recovered.

Fosamax Side Effects Report #5729606-4
Physician from UNITED KINGDOM reported FOSAMAX problem on Apr 28, 2008. Female patient, 70 years of age, was diagnosed with osteoporosis, blood cholesterol increased, hypothyroidism and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, blood thyroid stimulating hormone decreased, bruxism, chest pain, edentulous, jaw disorder, melanocytic naevus, mitral valve prolapse, osteonecrosis, . FOSAMAX dosage: unknown. During the same period patient was treated with RISEDRONATE, ATORVASTATIN, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5746599-4
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 26, 2008. Female patient, weighting 185.2 lb, was diagnosed with crohn's disease, pregnancy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemorrhage, labour complication, nasopharyngitis, pyrexia, streptococcal identification test positive, urinary tract infection, vulvovaginal mycotic infection, . HUMIRA dosage: unknown. During the same period patient was treated with VITAMIN, REMICADE, PREDNISONE. Patient recovered.

Arava Side Effects Report #5700618-X
Consumer or non-health professional from AUSTRALIA reported ARAVA problem on Apr 02, 2008. Female patient, 58 years of age, was diagnosed with rheumatoid arthritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, paralysis, rheumatoid factor increased, . ARAVA dosage: unknown. During the same period patient was treated with SALAZOPYRIN, PREDNISOLONE. Patient recovered.

Clozaril Side Effects Report #5717253-X
CLOZARIL problem was reported by a Health Professional from IRELAND on Apr 15, 2008. Male patient, 57 years of age, was diagnosed with schizophrenia and was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, choreoathetosis, confusional state, fatigue, gamma-glutamyltransferase increased, neutrophil count increased, transferrin saturation decreased, urinary incontinence, white blood cell count increased, . CLOZARIL dosage: 650 MG, QD. During the same period patient was treated with FOLIC ACID, ZYPREXA, VALPROATE. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5717751-9
Consumer or non-health professional from AUSTRALIA reported ARAVA problem on Apr 21, 2008. Female patient, 58 years of age, was diagnosed with rheumatoid arthritis and was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, paralysis, rheumatoid factor increased, . ARAVA dosage: unknown. During the same period patient was treated with SALAZOPYRIN, PREDNISOLONE. Patient recovered.

Dilantin Side Effects Report #5722874-4
DILANTIN problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 14, 2008. Male patient, 38 years of age, was diagnosed with convulsion and was treated with DILANTIN. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, convulsion, dysphagia, gastrooesophageal reflux disease, oesophageal haemorrhage, . DILANTIN dosage: 100 MG. During the same period patient was treated with PHENYTOIN. Patient recovered.

Nexium Side Effects Report #5723279-2
Pharmacist from UNITED STATES reported NEXIUM problem on Feb 11, 2008. Female patient, 58 years of age, was diagnosed with gastrooesophageal reflux disease and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, fatigue, . NEXIUM dosage: unknown. During the same period patient was treated with CRESTOR, CARDIZEM CD. Patient recovered.

Namenda Side Effects Report #5726253-5
NAMENDA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 23, 2008. Female patient, 83 years of age, was diagnosed with dementia and was treated with NAMENDA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, full blood count decreased, muscular weakness, tremor, . NAMENDA dosage: 20 MG QHS PO. During the same period patient was treated with PLAVIX, FOLTX, LOVASTATIN, ASPIRIN. Patient recovered.

Pantoprazole Side Effects Report #5364021-7
Consumer or non-health professional from AUSTRALIA reported PANTOPRAZOLE problem on June 18, 2007. Female patient, 75 years of age, was treated with PANTOPRAZOLE. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemorrhage, . PANTOPRAZOLE dosage: unknown. Patient was hospitalized. Patient recovered.

Pantoprazole Side Effects Report #5373210-7
PANTOPRAZOLE problem was reported by a Health Professional from AUSTRALIA on June 22, 2007. Female patient, 75 years of age, was treated with PANTOPRAZOLE. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, haemorrhage, . PANTOPRAZOLE dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5323063-8
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Apr 23, 2007. Female patient, 62 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, cystitis, dehydration, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5330194-5
REBIF problem was reported by a Physician from UNITED STATES on May 01, 2007. Male patient, 34 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, pneumonia, red blood cell count decreased, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5333349-9
Physician from UNITED STATES reported ENBREL problem on May 10, 2007. Female patient, weighting 159.8 lb, was diagnosed with polyarthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, syncope, vaginal haemorrhage, . ENBREL dosage: unknown. During the same period patient was treated with GLYBURIDE, ALLEGRA, NEURONTIN, TRAMADOL. Patient recovered.

Byetta Side Effects Report #5378058-5
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 16, 2007. Male patient, 80 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, . BYETTA dosage: unknown. Patient recovered.

Byetta Side Effects Report #5293944-2
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Mar 27, 2007. Female patient, 63 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, decreased appetite, gallbladder disorder, injection site erythema, injection site pruritus, loss of consciousness, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, ACTOS. Patient recovered.

Nisis Side Effects Report #5309348-X
NISIS problem was reported by a Consumer or non-health professional from FRANCE on Apr 16, 2007. Female patient, 79 years of age, weighting 94.80 lb, was diagnosed with hypertension and was treated with NISIS. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, gastritis atrophic, gastrointestinal haemorrhage, haematocrit decreased, haemoglobin decreased, iron deficiency anaemia, red blood cell count decreased, serum ferritin decreased, . NISIS dosage: 160 MG, QD. During the same period patient was treated with CORDARONE, HYPERIUM, DAFALGAN, ESOMEPRAZOLE MAGNESIUM. Patient recovered.

Cialis Side Effects Report #5261612-9
Consumer or non-health professional from UNITED STATES reported CIALIS problem on Sept 22, 2006. Male patient, 40 years of age, weighting 205.5 lb, was diagnosed with erectile dysfunction and was treated with CIALIS. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, spontaneous penile erection, therapeutic response decreased, therapeutic response delayed, . CIALIS dosage: 20 MG, ORAL. During the same period patient was treated with ENZYTE, PAXIL, BEXTRA, DETROL LA, AMBIEN, FERREX. Patient recovered.

Lamisil Side Effects Report #5261856-6
LAMISIL problem was reported by a Pharmacist from UNITED STATES on Feb 26, 2007. Male patient, 73 years of age, was diagnosed with onychomycosis and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, melaena, . LAMISIL dosage: 250 MG, QD. During the same period patient was treated with CARAFATE. Patient recovered.

Sudafed Side Effects Report #5274733-1
Consumer or non-health professional from UNITED STATES reported SUDAFED PE SINUS AND ALLERGY problem on Mar 08, 2007. Female patient, 43 years of age, weighting 200.0 lb, was diagnosed with sinus disorder and was treated with SUDAFED PE SINUS AND ALLERGY. After drug was administered, patient experienced the following problems/side effects: blood iron decreased, dizziness, flushing, heart rate increased, presyncope, speech disorder, vertigo, . SUDAFED PE SINUS AND ALLERGY dosage: unknown. Patient recovered.