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DYSPNOEA ( 19 FDA reports)
DRUG INEFFECTIVE ( 12 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
ASTHMA ( 7 FDA reports)
DRY MOUTH ( 6 FDA reports)
PAIN IN EXTREMITY ( 6 FDA reports)
AGEUSIA ( 5 FDA reports)
ARTHRALGIA ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
DYSPHONIA ( 5 FDA reports)
HEADACHE ( 5 FDA reports)
HYPOAESTHESIA ( 5 FDA reports)
ASTHENIA ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
INJECTION SITE ERYTHEMA ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
PNEUMONIA ( 4 FDA reports)
TREMOR ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
ABDOMINAL PAIN ( 3 FDA reports)
ALOPECIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
DIARRHOEA ( 3 FDA reports)
INJECTION SITE IRRITATION ( 3 FDA reports)
INJECTION SITE PAIN ( 3 FDA reports)
MULTIPLE SCLEROSIS ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
PAIN ( 3 FDA reports)
PAIN IN JAW ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
URINARY RETENTION ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BREAKTHROUGH PAIN ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CRANIAL NERVE DISORDER ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
DYSPNOEA EXACERBATED ( 2 FDA reports)
EXERCISE TOLERANCE DECREASED ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
HYPERSENSITIVITY ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INJECTION SITE PRURITUS ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
OPTIC NEURITIS ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
POLLAKIURIA ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RASH ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TRANSAMINASES INCREASED ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLOOD DISORDER ( 1 FDA reports)
BLOOD IMMUNOGLOBULIN E INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BREAST CANCER FEMALE ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY DISEASE ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CERVIX CARCINOMA ( 1 FDA reports)
CHEILITIS ( 1 FDA reports)
CHEST DISCOMFORT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHRONIC SINUSITIS ( 1 FDA reports)
CIRCUMORAL OEDEMA ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COLOUR BLINDNESS ( 1 FDA reports)
COUGH ( 1 FDA reports)
CREST SYNDROME ( 1 FDA reports)
CULTURE URINE POSITIVE ( 1 FDA reports)
CYSTOCELE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSPNOEA AT REST ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
ELECTROCARDIOGRAM CHANGE ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
EYE ROLLING ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING COLD ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FOETAL HEART RATE DECREASED ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GENITAL DISORDER FEMALE ( 1 FDA reports)
GESTATIONAL DIABETES ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GLIOMA ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GROIN PAIN ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE DECREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HIGH RISK PREGNANCY ( 1 FDA reports)
HOARSENESS ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOPARATHYROIDISM ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LEUKOPLAKIA ORAL ( 1 FDA reports)
LIP EXFOLIATION ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MACULAR HOLE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MICTURITION DISORDER ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE STRAIN ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEUROMYELITIS OPTICA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODULE ( 1 FDA reports)
OBSTRUCTIVE CHRONIC BRONCHITIS WITH ACUTE EXACERBATION ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PANCREATITIS ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PROSTATE EXAMINATION ABNORMAL ( 1 FDA reports)
PRURITUS ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PYURIA ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RECTOCELE ( 1 FDA reports)
RENAL CYST ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
SARCOIDOSIS ( 1 FDA reports)
SHARED PSYCHOTIC DISORDER ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOSIS ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT DISORDER ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINAL MUCOSAL BLISTERING ( 1 FDA reports)
VENTRICULAR DYSFUNCTION ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL ACUITY REDUCED ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
WHEELCHAIR USER ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

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