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INJECTION SITE ERYTHEMA ( 120 FDA reports)
INJECTION SITE INDURATION ( 76 FDA reports)
FALSE POSITIVE TUBERCULOSIS TEST ( 68 FDA reports)
INJECTION SITE PRURITUS ( 52 FDA reports)
INJECTION SITE RASH ( 30 FDA reports)
INJECTION SITE SWELLING ( 30 FDA reports)
INJECTION SITE PAIN ( 27 FDA reports)
INJECTION SITE WARMTH ( 23 FDA reports)
HYPERSENSITIVITY ( 21 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 20 FDA reports)
INCORRECT DOSE ADMINISTERED ( 18 FDA reports)
ERYTHEMA ( 16 FDA reports)
INJECTION SITE IRRITATION ( 16 FDA reports)
PAIN IN EXTREMITY ( 15 FDA reports)
PRURITUS ( 14 FDA reports)
INJECTION SITE URTICARIA ( 13 FDA reports)
RASH ERYTHEMATOUS ( 13 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 11 FDA reports)
NO ADVERSE DRUG REACTION ( 10 FDA reports)
INJECTION SITE VESICLES ( 9 FDA reports)
WRONG DRUG ADMINISTERED ( 9 FDA reports)
ACCIDENTAL EXPOSURE ( 7 FDA reports)
ANAPHYLACTIC REACTION ( 7 FDA reports)
ARTHRALGIA ( 7 FDA reports)
INDURATION ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
PYREXIA ( 7 FDA reports)
BLISTER ( 6 FDA reports)
CHEST PAIN ( 6 FDA reports)
DYSPNOEA ( 6 FDA reports)
HYPOAESTHESIA ( 6 FDA reports)
INJECTION SITE REACTION ( 6 FDA reports)
PRURITUS ALLERGIC ( 6 FDA reports)
DIZZINESS ( 5 FDA reports)
LOCALISED OEDEMA ( 5 FDA reports)
RASH ( 5 FDA reports)
TUBERCULIN TEST POSITIVE ( 5 FDA reports)
TUBERCULOSIS SKIN TEST POSITIVE ( 5 FDA reports)
ARTHRITIS ( 4 FDA reports)
DEATH ( 4 FDA reports)
HEART RATE INCREASED ( 4 FDA reports)
LOCAL REACTION ( 4 FDA reports)
PAIN ( 4 FDA reports)
SWELLING ( 4 FDA reports)
ASTHENIA ( 3 FDA reports)
CELLULITIS ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHILLS ( 3 FDA reports)
ERYTHEMA MULTIFORME ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
HEADACHE ( 3 FDA reports)
INJECTION SITE DISCOLOURATION ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
LYMPHADENOPATHY ( 3 FDA reports)
MALAISE ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
NAUSEA ( 3 FDA reports)
OEDEMA PERIPHERAL ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
SKIN EXFOLIATION ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ACTIVATED PARTIAL THROMBOPLASTIN TIME PROLONGED ( 2 FDA reports)
APPLICATION SITE REACTION ( 2 FDA reports)
BACK PAIN ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BLOOD CREATININE INCREASED ( 2 FDA reports)
BLOOD UREA INCREASED ( 2 FDA reports)
CONDITION AGGRAVATED ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
DYSPHONIA ( 2 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 2 FDA reports)
FAECAL OCCULT BLOOD POSITIVE ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
INJECTION SITE ABSCESS ( 2 FDA reports)
INJECTION SITE CELLULITIS ( 2 FDA reports)
INJECTION SITE NECROSIS ( 2 FDA reports)
INJECTION SITE SCAR ( 2 FDA reports)
JOINT SWELLING ( 2 FDA reports)
LYMPHADENITIS ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
PARAESTHESIA ORAL ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
PRE-EXISTING DISEASE ( 2 FDA reports)
PRODUCT CONTAMINATION MICROBIAL ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROTHROMBIN TIME PROLONGED ( 2 FDA reports)
RASH MACULAR ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
SCAR ( 2 FDA reports)
SKIN BACTERIAL INFECTION ( 2 FDA reports)
TENDERNESS ( 2 FDA reports)
THYROID DISORDER ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABDOMINAL PAIN UPPER ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ABSCESS ( 1 FDA reports)
ACANTHOSIS ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PSYCHOSIS ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
AORTIC DISORDER ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPIRATION TRACHEAL ABNORMAL ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BILIARY DYSKINESIA ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD FIBRINOGEN INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BREAST ABSCESS ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CLONUS ( 1 FDA reports)
COLD SWEAT ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONVULSION ( 1 FDA reports)
CROUP INFECTIOUS ( 1 FDA reports)
CUSHINGOID ( 1 FDA reports)
DELIVERY ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DERMATOMYOSITIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXPOSURE TO CONTAMINATED DEVICE ( 1 FDA reports)
EYE PAIN ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
FALL ( 1 FDA reports)
FEELING ABNORMAL ( 1 FDA reports)
FIBRIN D DIMER INCREASED ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FUNGAL INFECTION ( 1 FDA reports)
GALLBLADDER DISORDER ( 1 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 1 FDA reports)
GRANULOMA ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
ILEUS ( 1 FDA reports)
IMMUNE RECONSTITUTION SYNDROME ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE BRUISING ( 1 FDA reports)
INJECTION SITE CYST ( 1 FDA reports)
INJECTION SITE DISCOMFORT ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INFLAMMATION ( 1 FDA reports)
INJECTION SITE OEDEMA ( 1 FDA reports)
INSOMNIA ( 1 FDA reports)
KOEBNER PHENOMENON ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LUNG HYPERINFLATION ( 1 FDA reports)
LYMPH NODE PAIN ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICATION ERROR ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NEEDLE ISSUE ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PAPULE ( 1 FDA reports)
PARAKERATOSIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARESIS ( 1 FDA reports)
PATHOGEN RESISTANCE ( 1 FDA reports)
PEPTOSTREPTOCOCCUS INFECTION ( 1 FDA reports)
PHARYNGITIS STREPTOCOCCAL ( 1 FDA reports)
PHOTOPHOBIA ( 1 FDA reports)
PITUITARY CYST ( 1 FDA reports)
PLATELET COUNT INCREASED ( 1 FDA reports)
PRODUCT CONTAMINATION ( 1 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 1 FDA reports)
PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ( 1 FDA reports)
PROTEIN URINE PRESENT ( 1 FDA reports)
PROTEUS INFECTION ( 1 FDA reports)
PRURIGO ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
PYODERMA GANGRENOSUM ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
REFLEXES ABNORMAL ( 1 FDA reports)
REFUSAL OF TREATMENT BY PATIENT ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
SCARLET FEVER ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SIMILAR REACTION ON PREVIOUS EXPOSURE TO DRUG ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN FRAGILITY ( 1 FDA reports)
SKIN HYPERPIGMENTATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN OEDEMA ( 1 FDA reports)
SKIN REACTION ( 1 FDA reports)
SKIN TEST POSITIVE ( 1 FDA reports)
SKIN WARM ( 1 FDA reports)
SPUTUM CULTURE POSITIVE ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TREMOR ( 1 FDA reports)
TUBERCULOSIS ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VISUAL FIELD TESTS ABNORMAL ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
WOUND INFECTION STAPHYLOCOCCAL ( 1 FDA reports)

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