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FACIAL PARESIS side effect

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Cipro Side Effects Report #5626314-5
Consumer or non-health professional from ITALY reported CIPRO HC problem on Jan 30, 2008. Female patient, 41 years of age, was diagnosed with otitis media and was treated with CIPRO HC. After drug was administered, patient experienced the following problems/side effects: facial paresis, tympanic membrane perforation, . CIPRO HC dosage: unknown. Patient was hospitalized. Patient recovered.

Botox Side Effects Report #5639318-3
BOTOX problem was reported by a Physician from UNITED STATES on Feb 19, 2008. Female patient was diagnosed with facial paresis and was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: facial paresis, . BOTOX dosage: unknown. Patient recovered.

Botox Side Effects Report #5641008-8
Physician from GERMANY reported BOTOX problem on Feb 21, 2008. Female patient, weighting 207.2 lb, was diagnosed with hypertonic bladder, hypertension and was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: facial paresis, . BOTOX dosage: unknown. During the same period patient was treated with RAMIPRIL. Patient recovered.

Mirena Side Effects Report #5570432-7
MIRENA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 14, 2007. Female patient, 48 years of age, weighting 180.8 lb, was diagnosed with menorrhagia and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: facial paresis, hypoaesthesia, hypoaesthesia facial, muscular weakness, post procedural discomfort, transient ischaemic attack, . MIRENA dosage: unknown. Patient recovered.


Enbrel Side Effects Report #5510122-X
Physician from SWITZERLAND reported ENBREL problem on Oct 29, 2007. Male patient, 27 years of age, was diagnosed with psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: facial paresis, headache, herpes virus infection, nystagmus, pleocytosis, pyrexia, tinnitus, . ENBREL dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Botox Side Effects Report #5449002-7
BOTOX COSMETIC problem was reported by a Physician from UNITED STATES on Sept 06, 2007. Female patient was diagnosed with skin wrinkling and was treated with BOTOX COSMETIC. After drug was administered, patient experienced the following problems/side effects: facial paresis, . BOTOX COSMETIC dosage: unknown. Patient recovered.

Enbrel Side Effects Report #5449005-2
Physician from SWITZERLAND reported ENBREL problem on Aug 31, 2007. Male patient, 27 years of age, was diagnosed with psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: facial paresis, headache, herpes virus infection, nystagmus, pleocytosis, pyrexia, tinnitus, . ENBREL dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Enbrel Side Effects Report #5425898-X
ENBREL problem was reported by a Health Professional from SWITZERLAND on Aug 21, 2007. Male patient, 27 years of age, was diagnosed with psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: facial paresis, herpes virus infection, . ENBREL dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Humira Side Effects Report #5769580-8
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Apr 28, 2008. Male patient, weighting 145.1 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: facial paresis, muscular weakness, paraesthesia, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE. Patient recovered.


Humira Side Effects Report #5736775-9
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on May 05, 2008. Female patient, 71 years of age, weighting 169.8 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: facial paresis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISOLONE, NSAID. Patient was hospitalized. Patient recovered.

Zithromax Side Effects Report #5739414-6
Physician from GERMANY reported ZITHROMAX problem on May 06, 2008. Male patient, 18 years of age, was diagnosed with nasopharyngitis and was treated with ZITHROMAX. After drug was administered, patient experienced the following problems/side effects: facial paresis, . ZITHROMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Ultravist Side Effects Report #5741674-2
ULTRAVIST problem was reported by a Health Professional from UNITED STATES on Nov 07, 2006. Female patient, 43 years of age, was diagnosed with computerised tomogram abdomen and was treated with ULTRAVIST. After drug was administered, patient experienced the following problems/side effects: facial paresis, nausea, vomiting, . ULTRAVIST dosage: UNIT DOSE: 95 ML. Patient recovered.

Humira Side Effects Report #5752317-6
Consumer or non-health professional from GERMANY reported HUMIRA problem on May 20, 2008. Female patient, 71 years of age, weighting 169.8 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: facial paresis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISOLONE, NSAID. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5718302-5
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on Apr 17, 2008. Female patient, 71 years of age, weighting 169.8 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: facial paresis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISOLONE, NSAID. Patient was hospitalized. Patient recovered.


Forteo Side Effects Report #5316831-X
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Apr 23, 2007. Female patient, 87 years of age, was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: facial paresis, fall, ill-defined disorder, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Citalopram Side Effects Report #5329724-9
CITALOPRAM HYDROBROMIDE problem was reported by a Health Professional from DENMARK on Apr 30, 2007. Male patient, 82 years of age, was diagnosed with depression, panic attack and was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: facial paresis, hallucination, oedema mouth, tremor, . CITALOPRAM HYDROBROMIDE dosage: 10 MG QD PO. During the same period patient was treated with CITALOPRAM HYDROBROMIDE. Patient recovered.

Isotretinoin Side Effects Report #5292202-X
Physician from AUSTRIA reported ISOTRETINOIN problem on Apr 09, 2007. Male patient, 54 years of age, weighting 202.8 lb, was diagnosed with malignant melanoma and was treated with ISOTRETINOIN. After drug was administered, patient experienced the following problems/side effects: facial paresis, malignant melanoma, . ISOTRETINOIN dosage: unknown. During the same period patient was treated with ROFERON. Patient was hospitalized. Patient died on 09/10/2000.

Forteo Side Effects Report #5295989-5
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 02, 2007. Female patient, 87 years of age, was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: facial paresis, fall, ill-defined disorder, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Crestor Side Effects Report #5233588-1
Consumer or non-health professional from UNITED STATES reported CRESTOR problem on Apr 21, 2006. Female patient, 45 years of age, weighting 128.0 lb, was diagnosed with hypercholesterolaemia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: facial paresis, fatigue, muscular weakness, speech disorder, . CRESTOR dosage: 10 MG QD TPL. During the same period patient was treated with LABETALOL, INSULIN, ASPIRIN. Patient recovered.


Aggrenox Side Effects Report #5255600-6
AGGRENOX problem was reported by a Consumer or non-health professional from UNITED STATES on May 30, 2006. Female patient, weighting 121.0 lb, was diagnosed with cerebrovascular accident prophylaxis, hypertension, headache, insomnia and was treated with AGGRENOX. After drug was administered, patient experienced the following problems/side effects: facial paresis, headache, muscular weakness, . AGGRENOX dosage: unknown. During the same period patient was treated with MICARDIS, CLOPIDOGREL, HYDROCHLORITHIAZIDE, NORTRIPTYLINE, AMBIEN. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5269181-4
Consumer or non-health professional from BRAZIL reported BETASERON problem on Mar 05, 2007. Female patient, 35 years of age, was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: facial paresis, hemiplegia, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Botox Side Effects Report #5680659-1
BOTOX COSMETIC problem was reported by a Physician from UNITED STATES on Mar 21, 2008. Female patient was diagnosed with skin wrinkling and was treated with BOTOX COSMETIC. After drug was administered, patient experienced the following problems/side effects: dysphagia, facial paresis, . BOTOX COSMETIC dosage: unknown. Patient recovered.

Accuretic Side Effects Report #5509624-1
Consumer or non-health professional from ITALY reported ACCURETIC problem on Oct 31, 2007. Male patient, 66 years of age, was diagnosed with prostate cancer, metastases to bone and was treated with ACCURETIC. After drug was administered, patient experienced the following problems/side effects: bone lesion, facial paresis, hypoaesthesia, osteonecrosis, wound treatment, . ACCURETIC dosage: 20 MG/DIE, UNK. During the same period patient was treated with CASODEX, ZOMETA. Patient was hospitalized. Patient recovered.

Enbrel Side Effects Report #5522005-X
ENBREL problem was reported by a Physician from SWITZERLAND on Nov 09, 2007. Male patient, 27 years of age, weighting 198.4 lb, was diagnosed with psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: deafness neurosensory, facial paresis, headache, herpes virus infection, nystagmus, pleocytosis, pyrexia, tinnitus, . ENBREL dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Gleevec Side Effects Report #5527469-3
Physician from GERMANY reported GLEEVEC problem on Nov 22, 2007. Female patient, 38 years of age, weighting 158.7 lb, was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: dysarthria, facial paresis, hemiplegia, ischaemic cerebral infarction, raynaud's phenomenon, . GLEEVEC dosage: 400 MG, QD. Patient recovered.

Propranolol Side Effects Report #5477559-9
PROPRANOLOL problem was reported by a Physician from UNITED KINGDOM on Sept 20, 2007. Female patient, 19 years of age, was diagnosed with migraine and was treated with PROPRANOLOL. After drug was administered, patient experienced the following problems/side effects: dysarthria, facial paresis, muscular weakness, . PROPRANOLOL dosage: 80 MG;QD;PO. Patient was hospitalized. Patient recovered.

Accuretic Side Effects Report #5481282-4
Consumer or non-health professional from ITALY reported ACCURETIC problem on Oct 04, 2007. Male patient, 66 years of age, was diagnosed with prostate cancer, metastases to bone and was treated with ACCURETIC. After drug was administered, patient experienced the following problems/side effects: bone lesion, facial paresis, hypoaesthesia, osteonecrosis, wound treatment, . ACCURETIC dosage: 20 MG/DIE, UNK. During the same period patient was treated with CASODEX, ZOMETA. Patient was hospitalized. Patient recovered.

Perindopril Side Effects Report #5465337-6
PERINDOPRIL ERBUMINE problem was reported by a Health Professional from UNITED KINGDOM on Sept 13, 2007. Female patient, 60 years of age, was diagnosed with ill-defined disorder and was treated with PERINDOPRIL ERBUMINE. After drug was administered, patient experienced the following problems/side effects: angioedema, facial paresis, hypoaesthesia, oedema peripheral, paraesthesia, . PERINDOPRIL ERBUMINE dosage: DAILY DOSE: 8 MILLIGRAM(S). During the same period patient was treated with AMOXICILLIN, ASPIRIN, CODEINE SUL, INDAPAMIDE, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Propranolol Side Effects Report #5467656-6
Consumer or non-health professional from UNITED KINGDOM reported PROPRANOLOL problem on Sept 11, 2007. Female patient, 19 years of age, was diagnosed with migraine and was treated with PROPRANOLOL. After drug was administered, patient experienced the following problems/side effects: dysarthria, facial paresis, muscular weakness, . PROPRANOLOL dosage: 80 MG, ORAL. Patient was hospitalized. Patient recovered.

Propranolol Side Effects Report #5469403-0
PROPRANOLOL problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Sept 11, 2007. Female patient, 19 years of age, was diagnosed with migraine and was treated with PROPRANOLOL. After drug was administered, patient experienced the following problems/side effects: dysarthria, facial paresis, muscular weakness, . PROPRANOLOL dosage: (80 MG). Patient was hospitalized. Patient recovered.

Propranolol Side Effects Report #5470342-X
Health Professional from UNITED KINGDOM reported PROPRANOLOL problem on Sept 11, 2007. Female patient, 19 years of age, was diagnosed with migraine and was treated with PROPRANOLOL. After drug was administered, patient experienced the following problems/side effects: dysarthria, facial paresis, muscular weakness, . PROPRANOLOL dosage: 80 MG;QD;PO. Patient was hospitalized. Patient recovered.

Propranolol Side Effects Report #5470345-5
PROPRANOLOL problem was reported by a Physician from UNITED KINGDOM on Sept 13, 2007. Female patient, 19 years of age, was diagnosed with migraine and was treated with PROPRANOLOL. After drug was administered, patient experienced the following problems/side effects: dysarthria, facial paresis, muscular weakness, . PROPRANOLOL dosage: 80 MG; QD; PO. Patient was hospitalized. Patient recovered.

Propranolol Side Effects Report #5470720-9
Health Professional from UNITED KINGDOM reported PROPRANOLOL HYDROCHLORIDE problem on Sept 20, 2007. Female patient, 19 years of age, was diagnosed with migraine and was treated with PROPRANOLOL HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: dysarthria, facial paresis, muscular weakness, . PROPRANOLOL HYDROCHLORIDE dosage: 80 MG. Patient was hospitalized. Patient recovered.

Mirena Side Effects Report #5762205-7
MIRENA problem was reported by a Consumer or non-health professional from UNITED STATES on June 06, 2008. Female patient, 48 years of age, weighting 180.8 lb, was diagnosed with menorrhagia and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: complication of device insertion, facial paresis, hypoaesthesia, hypoaesthesia facial, muscular weakness, transient ischaemic attack, . MIRENA dosage: unknown. Patient recovered.

Mirena Side Effects Report #5778074-5
Consumer or non-health professional from UNITED STATES reported MIRENA problem on June 12, 2008. Female patient, 48 years of age, weighting 180.8 lb, was diagnosed with menorrhagia and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: complication of device insertion, facial paresis, hypoaesthesia, hypoaesthesia facial, muscular weakness, transient ischaemic attack, . MIRENA dosage: unknown. Patient recovered.

Propofol Side Effects Report #5781818-X
PROPOFOL problem was reported by a Consumer or non-health professional from UNITED KINGDOM on June 09, 2008. Male patient was diagnosed with nerve block and was treated with PROPOFOL. After drug was administered, patient experienced the following problems/side effects: dysarthria, facial paresis, hypoaesthesia, hypoglossal nerve disorder, migraine with aura, mobility decreased, muscular weakness, post procedural complication, . PROPOFOL dosage: 200 MG, ONCE. During the same period patient was treated with OXYGEN, SEVOFLURANE, FENTANYL. Patient recovered.

Lexapro Side Effects Report #5354503-6
Health Professional from NETHERLANDS reported LEXAPRO problem on May 28, 2007. Female patient, 35 years of age, weighting 143.3 lb, was diagnosed with depression and was treated with LEXAPRO. After drug was administered, patient experienced the following problems/side effects: depression, facial paresis, sinusitis, . LEXAPRO dosage: 20 MG QD PO. Patient recovered.

Humira Side Effects Report #5319539-X
HUMIRA problem was reported by a Health Professional from UNITED KINGDOM on May 01, 2007. Female patient, 57 years of age, weighting 154.3 lb, was diagnosed with pain and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: facial paresis, hypoaesthesia facial, paraesthesia, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, OMEPRAZOLE, DOSULEPIN, ESTROGENS CONJUGATED, TRAMADOL, ACETAMINOPHEN AND CODEINE PHOSPHATE. Patient recovered.

Citalopram Side Effects Report #5324708-9
Consumer or non-health professional from UNITED KINGDOM reported CITALOPRAM HYDROBROMIDE problem on Apr 27, 2007. Male patient, 82 years of age, was diagnosed with depression and was treated with CITALOPRAM HYDROBROMIDE. After drug was administered, patient experienced the following problems/side effects: dyskinesia, facial paresis, hallucination, oedema mouth, swelling, tremor, . CITALOPRAM HYDROBROMIDE dosage: 10 MG, QD, UNK. Patient recovered.

Natalizumab Side Effects Report #5339664-7
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on May 16, 2007. Female patient, 63 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: condition aggravated, facial paresis, multiple sclerosis, neuromyelitis optica, quadriparesis, . NATALIZUMAB dosage: 300 MG;QM;IV. During the same period patient was treated with LEVOXYL, BONIVA, AMBIEN. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5626703-9
Physician from UNITED KINGDOM reported HUMIRA problem on Feb 04, 2008. Female patient, weighting 108.9 lb, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: asthenia, demyelination, facial paresis, hypoaesthesia, hypoaesthesia facial, muscular weakness, sensory disturbance, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, INFLIXIMAB, HIGH DOSE STEROIDS, BUDESONIDE, LANSOPRAZOLE, ELECTROLADE, PARACETAMOL, PREDNISOLONE. Patient was hospitalized and became disabled. Patient recovered.

Tiotropium Side Effects Report #5599050-1
TIOTROPIUM problem was reported by a Consumer or non-health professional from on Jan 16, 2008. Male patient, 61 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with TIOTROPIUM. After drug was administered, patient experienced the following problems/side effects: dysarthria, face injury, facial paresis, hemicephalalgia, herpes zoster oticus, nausea, vertebrobasilar insufficiency, vertigo, vestibular disorder, . TIOTROPIUM dosage: unknown. Patient was hospitalized. Patient recovered.

Tiotropium Side Effects Report #5511840-X
Consumer or non-health professional from reported TIOTROPIUM problem on Nov 05, 2007. Male patient, 61 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with TIOTROPIUM. After drug was administered, patient experienced the following problems/side effects: dysarthria, face injury, facial paresis, hemicephalalgia, herpes zoster oticus, nausea, vertebrobasilar insufficiency, vertigo, vestibular disorder, . TIOTROPIUM dosage: unknown. Patient was hospitalized. Patient recovered.

Champix Side Effects Report #5475257-9
CHAMPIX problem was reported by a Consumer or non-health professional from SWITZERLAND on Sept 20, 2007. Male patient, 59 years of age, was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: arthropod bite, cerebrovascular accident, facial paresis, . CHAMPIX dosage: unknown. Patient was hospitalized. Patient recovered.

Champix Side Effects Report #5479099-X
Physician from SWITZERLAND reported CHAMPIX problem on Sept 20, 2007. Male patient, 59 years of age, was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: arthropod bite, cerebrovascular accident, facial paresis, . CHAMPIX dosage: unknown. Patient was hospitalized. Patient recovered.

Menactra Side Effects Report #5490483-0
MENACTRA problem was reported by a Health Professional from UNITED STATES on Oct 15, 2007. Male patient, 18 years of age, was diagnosed with immunisation, tuberculin test and was treated with MENACTRA. After drug was administered, patient experienced the following problems/side effects: areflexia, dysarthria, facial paresis, gait disturbance, guillain-barre syndrome, muscular weakness, neck pain, paraesthesia, sensation of heaviness, . MENACTRA dosage: unknown. During the same period patient was treated with TUBERSOL, DIFFERIN. Patient was hospitalized. Patient recovered.

Botox Side Effects Report #5403347-5
Consumer or non-health professional from UNITED STATES reported BOTOX problem on July 26, 2007. Female patient, 36 years of age, was diagnosed with facial spasm, temporomandibular joint syndrome, headache and was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: drooling, eye disorder, facial paresis, muscle spasms, muscular weakness, neck pain, skin burning sensation, therapeutic response decreased, trismus, . BOTOX dosage: unknown. Patient recovered.

Sorafenib Side Effects Report #5376931-5
SORAFENIB problem was reported by a Consumer or non-health professional from AUSTRIA on June 25, 2007. Male patient, 78 years of age, was diagnosed with neoplasm malignant and was treated with SORAFENIB. After drug was administered, patient experienced the following problems/side effects: cough, diarrhoea, facial paresis, rash, vomiting, . SORAFENIB dosage: TOTAL DAILY DOSE: 800 MG. During the same period patient was treated with THROMBO ASS. Patient was hospitalized. Patient recovered.

Sorafenib Side Effects Report #5376931-5
Consumer or non-health professional from AUSTRIA reported SORAFENIB problem on June 25, 2007. Male patient, 78 years of age, was diagnosed with neoplasm malignant and was treated with SORAFENIB. After drug was administered, patient experienced the following problems/side effects: cough, diarrhoea, facial paresis, rash, vomiting, . SORAFENIB dosage: TOTAL DAILY DOSE: 800 MG. During the same period patient was treated with THROMBO ASS. Patient was hospitalized. Patient recovered.

Botulinum Side Effects Report #5761988-X
BOTULINUM TOXIN TYPE B problem was reported by a Physician from PORTUGAL on May 20, 2008. Female patient was diagnosed with off label use, salivary hypersecretion and was treated with BOTULINUM TOXIN TYPE B. After drug was administered, patient experienced the following problems/side effects: back pain, eye irritation, facial paresis, mastication disorder, off label use, paraesthesia, pneumonia aspiration, respiratory tract infection, saliva altered, . BOTULINUM TOXIN TYPE B dosage: unknown. During the same period patient was treated with BOTULINUM TOXIN TYPE B, AMITRIPTYLINE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5780520-8
Health Professional from UNITED KINGDOM reported HUMIRA problem on June 13, 2008. Female patient, weighting 262.4 lb, was diagnosed with psoriatic arthropathy, uveitis, diabetes mellitus, nausea, hypothyroidism and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: demyelination, diplopia, facial paresis, paraesthesia, sensory disturbance, . HUMIRA dosage: unknown. During the same period patient was treated with METFORMIN, NOVOLOG, SIMVASTATIN, METOCLOPRAMIDE, BRUFEN RETARD, LEVOTHYROXINE. Patient was hospitalized and became disabled. Patient recovered.