Please choose an event type to view the corresponding MedsFacts report:

DRUG INEFFECTIVE ( 2764 FDA reports)
HERPES SIMPLEX ( 701 FDA reports)
ORAL HERPES ( 451 FDA reports)
SWELLING FACE ( 232 FDA reports)
INTENTIONAL DRUG MISUSE ( 151 FDA reports)
APPLICATION SITE IRRITATION ( 133 FDA reports)
HYPERSENSITIVITY ( 104 FDA reports)
LIP SWELLING ( 102 FDA reports)
APPLICATION SITE ERYTHEMA ( 80 FDA reports)
APPLICATION SITE PAIN ( 78 FDA reports)
APPLICATION SITE SWELLING ( 68 FDA reports)
CHEILITIS ( 68 FDA reports)
LIP PAIN ( 55 FDA reports)
BURNING SENSATION ( 54 FDA reports)
LIP DRY ( 47 FDA reports)
SCAR ( 47 FDA reports)
APPLICATION SITE BLEEDING ( 45 FDA reports)
CHAPPED LIPS ( 44 FDA reports)
APPLICATION SITE REACTION ( 41 FDA reports)
LIP HAEMORRHAGE ( 40 FDA reports)
DRUG ADMINISTRATION ERROR ( 36 FDA reports)
APPLICATION SITE SCAR ( 35 FDA reports)
LIP BLISTER ( 32 FDA reports)
PRURITUS ( 32 FDA reports)
RASH ( 32 FDA reports)
APPLICATION SITE PARAESTHESIA ( 31 FDA reports)
APPLICATION SITE DRYNESS ( 30 FDA reports)
ERYTHEMA ( 29 FDA reports)
SCAB ( 29 FDA reports)
PAIN ( 28 FDA reports)
APPLICATION SITE DISCOLOURATION ( 24 FDA reports)
APPLICATION SITE PRURITUS ( 24 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 23 FDA reports)
APPLICATION SITE VESICLES ( 22 FDA reports)
APPLICATION SITE SCAB ( 21 FDA reports)
HYPOAESTHESIA ORAL ( 20 FDA reports)
PARAESTHESIA ( 20 FDA reports)
IMPAIRED HEALING ( 19 FDA reports)
LIP DISORDER ( 18 FDA reports)
APPLICATION SITE INFECTION ( 17 FDA reports)
SKIN LACERATION ( 17 FDA reports)
LIP EXFOLIATION ( 15 FDA reports)
PARAESTHESIA ORAL ( 14 FDA reports)
URTICARIA ( 14 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
HYPOAESTHESIA ( 13 FDA reports)
LIP DISCOLOURATION ( 13 FDA reports)
APPLICATION SITE EXFOLIATION ( 12 FDA reports)
OEDEMA MOUTH ( 12 FDA reports)
DIZZINESS ( 11 FDA reports)
FACIAL PAIN ( 10 FDA reports)
BLISTER ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
EXPIRED DRUG ADMINISTERED ( 9 FDA reports)
EYE PAIN ( 9 FDA reports)
EYE SWELLING ( 9 FDA reports)
LOCAL SWELLING ( 9 FDA reports)
NONSPECIFIC REACTION ( 9 FDA reports)
SWELLING ( 9 FDA reports)
ANXIETY ( 8 FDA reports)
APPLICATION SITE ANAESTHESIA ( 8 FDA reports)
APPLICATION SITE BURN ( 8 FDA reports)
HYPOAESTHESIA FACIAL ( 8 FDA reports)
OCULAR HYPERAEMIA ( 8 FDA reports)
SPEECH DISORDER ( 8 FDA reports)
STOMATITIS ( 8 FDA reports)
APPLICATION SITE RASH ( 7 FDA reports)
INTENTIONAL MISUSE ( 7 FDA reports)
ORAL PAIN ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
APPLICATION SITE WARMTH ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
FEELING ABNORMAL ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
INSOMNIA ( 6 FDA reports)
LYMPHADENOPATHY ( 6 FDA reports)
NAIL DISORDER ( 6 FDA reports)
NO ADVERSE DRUG EFFECT ( 6 FDA reports)
PAIN IN JAW ( 6 FDA reports)
PIGMENTATION LIP ( 6 FDA reports)
SKIN IRRITATION ( 6 FDA reports)
SWOLLEN TONGUE ( 6 FDA reports)
APNOEA ( 5 FDA reports)
APPLICATION SITE DISCHARGE ( 5 FDA reports)
ATRIAL SEPTAL DEFECT ( 5 FDA reports)
BACTERIAL SEPSIS ( 5 FDA reports)
BRONCHOMALACIA ( 5 FDA reports)
DYSGEUSIA ( 5 FDA reports)
EXOMPHALOS ( 5 FDA reports)
FACE OEDEMA ( 5 FDA reports)
HAEMORRHAGE ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
INFECTION ( 5 FDA reports)
LARYNGOMALACIA ( 5 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 5 FDA reports)
LUNG DISORDER ( 5 FDA reports)
NAUSEA ( 5 FDA reports)
PATENT DUCTUS ARTERIOSUS ( 5 FDA reports)
PERSISTENT FOETAL CIRCULATION ( 5 FDA reports)
PNEUMONIA KLEBSIELLA ( 5 FDA reports)
RASH MACULAR ( 5 FDA reports)
RESPIRATORY FAILURE ( 5 FDA reports)
RIGHT VENTRICULAR HYPERTROPHY ( 5 FDA reports)
SKIN DISCOLOURATION ( 5 FDA reports)
TRACHEOMALACIA ( 5 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 5 FDA reports)
VOMITING ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
ACNE ( 4 FDA reports)
APPLICATION SITE INFLAMMATION ( 4 FDA reports)
APPLICATION SITE PAPULES ( 4 FDA reports)
COUGH ( 4 FDA reports)
DYSPHAGIA ( 4 FDA reports)
EYE IRRITATION ( 4 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 4 FDA reports)
MIGRAINE ( 4 FDA reports)
MOUTH ULCERATION ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
OEDEMA PERIPHERAL ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
ORAL MUCOSAL BLISTERING ( 4 FDA reports)
PALLOR ( 4 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 4 FDA reports)
PHARYNGEAL OEDEMA ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
SENSORY DISTURBANCE ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
TENSION ( 4 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 4 FDA reports)
THERMAL BURN ( 4 FDA reports)
TREATMENT NONCOMPLIANCE ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
APPLICATION SITE DERMATITIS ( 3 FDA reports)
APPLICATION SITE HYPERAESTHESIA ( 3 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 3 FDA reports)
BLOOD CALCIUM DECREASED ( 3 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 3 FDA reports)
BLOOD POTASSIUM DECREASED ( 3 FDA reports)
CAECITIS ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONGENITAL ANOMALY ( 3 FDA reports)
DERMATITIS ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DRY MOUTH ( 3 FDA reports)
DRY SKIN ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FACIAL PALSY ( 3 FDA reports)
FEAR ( 3 FDA reports)
FIBRIN D DIMER INCREASED ( 3 FDA reports)
HAEMATOCRIT DECREASED ( 3 FDA reports)
HAEMOGLOBIN DECREASED ( 3 FDA reports)
HEART DISEASE CONGENITAL ( 3 FDA reports)
HYPERAESTHESIA ( 3 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 3 FDA reports)
MECHANICAL VENTILATION ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PROTHROMBIN TIME PROLONGED ( 3 FDA reports)
SEPSIS ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
STREPTOCOCCAL INFECTION ( 3 FDA reports)
TRACHEAL DISORDER ( 3 FDA reports)
TREMOR ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
VISION BLURRED ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 3 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ALCOHOLISM ( 2 FDA reports)
ALPHA-1 ANTI-TRYPSIN DEFICIENCY ( 2 FDA reports)
APHASIA ( 2 FDA reports)
APPLICATION SITE ULCER ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
BACTERIA URINE ( 2 FDA reports)
BASAL CELL CARCINOMA ( 2 FDA reports)
BLOOD BLISTER ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 2 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 2 FDA reports)
BREAST CANCER ( 2 FDA reports)
BRONCHOPULMONARY DYSPLASIA ( 2 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CERVICAL DYSPLASIA ( 2 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 2 FDA reports)
CONSTIPATION ( 2 FDA reports)
CULTURE URINE POSITIVE ( 2 FDA reports)
DEHYDRATION ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
ELECTROCARDIOGRAM ST-T CHANGE ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYELID PTOSIS ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
FEAR OF DISEASE ( 2 FDA reports)
FLANK PAIN ( 2 FDA reports)
GASTROSCHISIS ( 2 FDA reports)
GINGIVITIS ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
GOUT ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HYPERTHYROIDISM ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
KLEBSIELLA INFECTION ( 2 FDA reports)
LIFE EXPECTANCY SHORTENED ( 2 FDA reports)
LOCALISED INFECTION ( 2 FDA reports)
LUNG CONSOLIDATION ( 2 FDA reports)
MALAISE ( 2 FDA reports)
MUSCLE SPASMS ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
NASAL OEDEMA ( 2 FDA reports)
NASOPHARYNGITIS ( 2 FDA reports)
OEDEMA ( 2 FDA reports)
OSTEITIS ( 2 FDA reports)
OSTEOPENIA ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
PSYCHIATRIC SYMPTOM ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RENAL FAILURE ( 2 FDA reports)
SKIN INDURATION ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
SKIN ULCER ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
TENDON DISORDER ( 2 FDA reports)
TRI-IODOTHYRONINE INCREASED ( 2 FDA reports)
UPPER RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
VITAMIN K DEFICIENCY ( 2 FDA reports)
WOUND HAEMORRHAGE ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AGEUSIA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APPLICATION SITE EXCORIATION ( 1 FDA reports)
APPLICATION SITE INDURATION ( 1 FDA reports)
ASTHENIA ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
BIOPSY ( 1 FDA reports)
BIOPSY BREAST ABNORMAL ( 1 FDA reports)
BLEEDING TIME PROLONGED ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLISTER INFECTED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BRAIN ABSCESS ( 1 FDA reports)
BREAST CANCER IN SITU ( 1 FDA reports)
BREAST LUMP REMOVAL ( 1 FDA reports)
BURNING SENSATION MUCOSAL ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CHEST PAIN ( 1 FDA reports)
CHILLS ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
DEATH ( 1 FDA reports)
DISCOMFORT ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR DISCOMFORT ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
EATING DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ST-T SEGMENT ABNORMAL ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
ENCEPHALITIS HERPES ( 1 FDA reports)
ENDOMETRIAL CANCER METASTATIC ( 1 FDA reports)
ERYTHEMA MULTIFORME ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYELID FUNCTION DISORDER ( 1 FDA reports)
EYELIDS PRURITUS ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FEELING JITTERY ( 1 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GENITAL RASH ( 1 FDA reports)
GINGIVAL DISCOLOURATION ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTRANASAL HYPOAESTHESIA ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
KERATITIS ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP PRURITUS ( 1 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
LYMPHADENECTOMY ( 1 FDA reports)
LYMPHADENITIS ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
METASTASES TO BONE ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MILIA ( 1 FDA reports)
MOLE EXCISION ( 1 FDA reports)
MOUTH INJURY ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE SCLEROSIS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OCHLOPHOBIA ( 1 FDA reports)
OEDEMA MUCOSAL ( 1 FDA reports)
OPEN WOUND ( 1 FDA reports)
ORAL DISCHARGE ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PHARYNGOLARYNGEAL DISCOMFORT ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PIGMENTATION DISORDER ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRURITUS GENITAL ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYELONEPHRITIS ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH PUSTULAR ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN DEPIGMENTATION ( 1 FDA reports)
SKIN INFLAMMATION ( 1 FDA reports)
SKIN INJURY ( 1 FDA reports)
SKIN TIGHTNESS ( 1 FDA reports)
SOFT TISSUE INFECTION ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPUTUM RETENTION ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA OF SKIN ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
SUBMANDIBULAR MASS ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SURGERY ( 1 FDA reports)
TESTICULAR SWELLING ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED WITH DRUG SUBSTITUTION ( 1 FDA reports)
THINKING ABNORMAL ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
URETHRAL PAIN ( 1 FDA reports)
URINARY HESITATION ( 1 FDA reports)
URINARY RETENTION ( 1 FDA reports)
UTERINE MASS ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHEEZING ( 1 FDA reports)

© 2014 MedsFacts, Inc
Privacy Policy
Terms of Use